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4316-53-4

4316-53-4

Identification

  • Molecular Formula:C19H17N

  • EINECS:677-549-3

Synonyms:(4-Methylphenyl)diphenylamine;4-Methyl-N,N-diphenylaniline;4-Methyl-N,N-diphenylbenzenamine;N-(4-Methylphenyl)-N,N-diphenylamine;

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Safety information and MSDS

  • Pictogram(s):

  • Hazard Codes:

  • Signal Word:

  • Hazard Statement:

  • First-aid measures: General adviceConsult a physician. Show this safety data sheet to the doctor in attendance.If inhaled If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician. In case of skin contact Wash off with soap and plenty of water. Consult a physician. In case of eye contact Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician. If swallowed Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.

  • Fire-fighting measures: Suitable extinguishing media Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Wear self-contained breathing apparatus for firefighting if necessary.

  • Accidental release measures: Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. For personal protection see section 8. Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Pick up and arrange disposal. Sweep up and shovel. Keep in suitable, closed containers for disposal.

  • Handling and storage: Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Avoid exposure - obtain special instructions before use.Provide appropriate exhaust ventilation at places where dust is formed. For precautions see section 2.2. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.

  • Exposure controls/personal protection:Occupational Exposure limit valuesBiological limit values Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and at the end of workday. Eye/face protection Safety glasses with side-shields conforming to EN166. Use equipment for eye protection tested and approved under appropriate government standards such as NIOSH (US) or EN 166(EU). Skin protection Wear impervious clothing. The type of protective equipment must be selected according to the concentration and amount of the dangerous substance at the specific workplace. Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique(without touching glove's outer surface) to avoid skin contact with this product. Dispose of contaminated gloves after use in accordance with applicable laws and good laboratory practices. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it. Respiratory protection Wear dust mask when handling large quantities. Thermal hazards

Supplier and reference price

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  • Manufacture/Brand:AK Scientific
  • Product Description:4-Methyl-N,N-diphenylaniline
  • Packaging:5g
  • Price:$ 546
  • Delivery:In stock
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  • Manufacture/Brand:Alichem
  • Product Description:4-Methyl-N,N-diphenylaniline
  • Packaging:500mg
  • Price:$ 798.7
  • Delivery:In stock
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  • Manufacture/Brand:Alichem
  • Product Description:4-Methyl-N,N-diphenylaniline
  • Packaging:1g
  • Price:$ 1490
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  • Manufacture/Brand:Alichem
  • Product Description:4-Methyl-N,N-diphenylaniline
  • Packaging:250mg
  • Price:$ 475.2
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  • Manufacture/Brand:Ambeed
  • Product Description:4-Methyl-N,N-diphenylaniline 98%
  • Packaging:100g
  • Price:$ 220
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  • Manufacture/Brand:Ambeed
  • Product Description:4-Methyl-N,N-diphenylaniline 98%
  • Packaging:5g
  • Price:$ 26
  • Delivery:In stock
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  • Manufacture/Brand:Ambeed
  • Product Description:4-Methyl-N,N-diphenylaniline 98%
  • Packaging:25g
  • Price:$ 69
  • Delivery:In stock
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  • Manufacture/Brand:American Custom Chemicals Corporation
  • Product Description:4-METHYLTRIPHENYLAMINE 95.00%
  • Packaging:5G
  • Price:$ 909.56
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  • Manufacture/Brand:Chemenu
  • Product Description:4-Methyl-N,N-diphenylaniline 95%
  • Packaging:10g
  • Price:$ 448
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  • Manufacture/Brand:Matrix Scientific
  • Product Description:4-Methyl-N,N-diphenylaniline 95+%
  • Packaging:1g
  • Price:$ 284
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Relevant articles and documentsAll total 85 Articles be found

Transition-Metal-Free Diarylation of Isocyanates with Arynes

Jang, Woo Cheol,Hwang, Dong Wook,Seo, Jeong Hoon,Ko, Haye Min

supporting information, (2019/08/30)

A facile method for the transition-metal-free diarylation of isocyanates with arynes in the presence of cesium fluoride has been developed, which affords functionalized diaryl amines in moderate to excellent yields. This reaction has good functional group tolerance and provides excellent regioselectivity by utilizing a methoxy-substituted aryne precursor.

PHOSPHINE COMPOUND, CROSSLINKED COMPOSITION, AND MANUFACTURING METHOD OF AROMATIC AMINE COMPOUND

-

Paragraph 0044-0046; 0047-0048, (2019/12/25)

PROBLEM TO BE SOLVED: To provide a phosphine compound capable of constituting a transition metal complex excellent in reaction speed and selectivity as a catalyst. SOLUTION: There is provided a phosphine compound represented by the formula (I). In the formula Ar represents each independently an aryl group which may be substituted, R1 represents each independently a linear, branched or cyclic alkyl group, R2 represents each independently a linear, branched or cyclic alkyl group, alkoxy group or aryl group which may be substituted, or neighboring 2 R2 are bound each other to form a ring, and n represents an integer of 0 to 4. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

DIARYL AMINE COMPOUND AND METHOD FOR PRODUCING THE SAME

-

Paragraph 0218; 0235-0237, (2021/03/16)

The present invention relates to a process for the preparation of diaryl amine compounds. A compound represented by chemical formula 1, a compound represented by chemical formula 2, and a synthetic reagent in a solvent, the synthetic reagent being CsF, KF, 18 - crown -6, K. 2 CO3, [TBAT] The present invention relates to a process for the preparation of diaryl amine compounds comprising a material selected from the group consisting of a (tetrabutylammonium difluorotriphenylsilicate), TBAF (tetrabutylammonium fluoride) and combinations thereof. Chemical Formula 1. Chemical Formula 2. The diaryl amine compound can be synthesized under the absence of a transition metal to be used to synthesize diaryl amine compounds having various substituents.

Design of Benzimidazolyl Phosphines Bearing AlterableP,OorP,N-Coordination: Synthesis, Characterization, and Insights into Their Reactivity

Wong, Shun Man,Choy, Pui Ying,Zhao, Qingyang,Yuen, On Ying,Yeung, Chung Chiu,So, Chau Ming,Kwong, Fuk Yee

supporting information, p. 2265 - 2271 (2021/05/05)

A new series of hemilabile benzimidazolyl phosphines is reported. Entities in this ligand family can be easily assembled and prepared on a large scale via a simple one-pot procedure. X-ray crystallographic analyses show that the Pd metal center can coordinate in different fashions, where it relies on the size of the ?PR2group. With the same ligand scaffold, the ligand having a ?PCy2moiety displays better efficiency in expediting aromatic C-C bond-coupling reactions, while the ligand associated with a ?P-t-Bu2group, in contrast, promotes C-N bond-forming reactions.

A Tetraarylpyrrole-Based Phosphine Ligand for the Palladium-Catalyzed Amination of Aryl Chlorides

Sai, Masahiro

supporting information, p. 5422 - 5428 (2021/10/08)

A tetraarylpyrrole-based phosphine ligand L1 in combination with Pd(dba)2 provided a catalyst for the Buchwald-Hartwig amination reaction. A variety of amines were rapidly coupled with aryl chlorides at a Pd loading of 0.5 mol%. The selective monoarylation of aliphatic primary amines was achieved in the presence of 0.8 equiv. water. Comparison experiments were also conducted, which revealed that the catalytic activity of L1 is superior to representative phosphine ligands in the Pd-catalyzed C?N coupling of various amines. (Figure presented.).

Process route upstream and downstream products

Process route

4-tolyl iodide
624-31-7

4-tolyl iodide

diphenylamine
122-39-4

diphenylamine

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

Conditions
ConditionsYield
96%
92%
Withpotassium tert-butylate;Intoluene;at 120 ℃; for 12h;
90%
88%
80%
79%
Withpotassium phosphate; 8-quinolinol; copper(l) chloride;InN,N-dimethyl-formamide;at 120 ℃; for 24h; Inert atmosphere;
76%
75%
WithCu(neocup)(PPh3)Br; potassium tert-butylate;Intoluene;at 110 - 120 ℃; for 6h;
70%
With[2,2]bipyridinyl; copper(l) iodide; potassium tert-butylate;Intoluene;at 100 ℃; for 24h; Inert atmosphere; Sealed tube;
69%
68%
61%
Withpotassium carbonate;copper; copper(l) chloride;Innitrobenzene;at 210 - 220 ℃; for 12h;
60%
52%
With[2,2]bipyridinyl; copper(l) iodide; potassium tert-butylate;Intetrahydrofuran; toluene;at 100 ℃; for 24h; Inert atmosphere;
51%
4-tolyl iodide;With1,10-Phenanthroline;Indimethylsulfoxide-d6;at 80 ℃; Concentration; Temperature; Reagent/catalyst; Kinetics; Inert atmosphere;
90 %Chromat.
99.1 %Chromat.
92.7 %Spectr.
Withcopper(l) iodide; 1,10-Phenanthroline; potassium tert-butylate;Intoluene;at 120 ℃; for 6h; Reagent/catalyst; Time;
99 %Chromat.
With18-crown-6 ether; copper; potassium carbonate;In1,2-dichloro-benzene;at 190 ℃; Inert atmosphere;
iodobenzene
591-50-4

iodobenzene

C<sub>7</sub>H<sub>8</sub>N<sup>(1-)</sup>*Br<sup>(1-)</sup>*Mg<sup>(2+)</sup>

C7H8N(1-)*Br(1-)*Mg(2+)

4-methyldiphenylamine
620-84-8

4-methyldiphenylamine

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

(E)-4,4'-dimethylazobenzene
501-60-0

(E)-4,4'-dimethylazobenzene

Conditions
ConditionsYield
With[2,2]bipyridinyl; copper(l) iodide;Inpyridine;for 24h; Heating;
14%
4%
73%
iodobenzene
591-50-4

iodobenzene

4-tolyl iodide
624-31-7

4-tolyl iodide

diphenylamine
122-39-4

diphenylamine

N,N-diphenylaminobenzene
603-34-9

N,N-diphenylaminobenzene

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

Conditions
ConditionsYield
potassium hydroxide; copper;at 160 ℃; Rate constant; Mechanism; competitive reaction, var. catalysts;
meta-bromotoluene
591-17-3

meta-bromotoluene

diphenylamine
122-39-4

diphenylamine

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

N,N-diphenyl-m-toluidine
4316-54-5

N,N-diphenyl-m-toluidine

2-methyl-N,N-diphenylaniline
4316-55-6

2-methyl-N,N-diphenylaniline

Conditions
ConditionsYield
Withpotassium hydroxide;PEGDM-400;Intoluene;at 161 - 163 ℃; for 8h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
para-bromotoluene
106-38-7

para-bromotoluene

diphenylamine
122-39-4

diphenylamine

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

N,N-diphenyl-m-toluidine
4316-54-5

N,N-diphenyl-m-toluidine

Conditions
ConditionsYield
Withpotassium hydroxide;PEGDM-400;Intoluene;at 165 ℃; for 8h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Withiron(III) oxide; potassium tert-butylate;Indimethyl sulfoxide;at 130 ℃; for 36h; regioselective reaction;
iodobenzene
591-50-4

iodobenzene

1-methyl-4-nitrobenzene
99-99-0

1-methyl-4-nitrobenzene

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

Conditions
ConditionsYield
Withcopper; at 195 ℃;
para-chlorotoluene
106-43-4

para-chlorotoluene

diphenylamine
122-39-4

diphenylamine

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

Conditions
ConditionsYield
99%
Withpalladium diacetate; sodium t-butanolate; ruphos;Inneat (no solvent);at 110 ℃; for 12h; Green chemistry;
99%
98%
96%
94%
94%
93%
91%
Withtris-(dibenzylideneacetone)dipalladium(0); C33H48N7P; sodium t-butanolate;Intoluene;at 80 ℃; for 24h; Inert atmosphere; Schlenk technique; Glovebox;
91%
Withbis[chloro(1,2,3-trihapto-allylbenzene)palladium(II)]; N-[2-(di(1-adamantyl)phosphino)phenyl]morpholine; sodium t-butanolate; at 110 ℃; for 21h; chemoselective reaction; Inert atmosphere; neat (no solvent);
90%
88%
82%
81%
80%
80%
76%
75%
para-chlorotoluene;Intetrahydrofuran; 1,4-dioxane;at 20 - 95 ℃; for 12.16h; Inert atmosphere;
65%
WithC37H50BrO3PPd;In1,4-dioxane;at 80 ℃; Kinetics; Inert atmosphere; Glovebox; Sealed tube;
iodobenzene
591-50-4

iodobenzene

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

Conditions
ConditionsYield
95%
82%
Withpotassium tert-butylate;Intoluene;at 120 ℃; for 14h; Inert atmosphere;
65%
para-bromotoluene
106-38-7

para-bromotoluene

diphenylamine
122-39-4

diphenylamine

diphenyl(p-tolyl)amine
4316-53-4

diphenyl(p-tolyl)amine

Conditions
ConditionsYield
Withpalladium diacetate; sodium t-butanolate; ruphos;Inneat (no solvent);at 110 ℃; for 12h; Green chemistry;
99%
97%
Withpotassium hydroxide;Inwater;for 24h; Reflux; Inert atmosphere;
95%
Withbis(η3-allyl-μ-chloropalladium(II)); potassium hydroxide;Inwater;for 24h; Reflux; Inert atmosphere;
95%
diphenylamine;Withethylmagnesium bromide;Indiethyl ether;at 0 - 40 ℃; for 2h; Inert atmosphere;
92%
91%
Withactive Cu;Inwater;microwave irradiation;
81%
Withpalladium diacetate; sodium t-butanolate; ruphos;Inneat (no solvent);at 110 ℃; for 12h; Inert atmosphere; Green chemistry;
81%
Withcesium fluoride; bis(dibenzylideneacetone)-palladium(0); XPhos; at 100 ℃; for 18h; Time; Inert atmosphere; Sealed tube;
80%
71%
Withwater; sodium t-butanolate;InN,N-dimethyl-formamide;at 120 ℃; for 3h; Schlenk technique;
70%
65%
Withsodium t-butanolate;Intoluene;at 70 ℃; for 24h; Inert atmosphere;
60%
Withpotassium hydroxide;[(t-Bu)2PCl]2PdCl2;Intoluene;at 20 ℃; for 5h; Conversion of starting material; Heating / reflux;
85.7 g

Global suppliers and manufacturers

Global( 67) Suppliers
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  • Amadis Chemical Co., Ltd.
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  • Career Henan Chemical Co
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