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Cas Database

4415-87-6

4415-87-6

Identification

  • Molecular Formula:C8H4O6

  • EINECS:224-577-5

Synonyms:1,2,3,4-Cyclobutanetetracarboxylic1,2:3,4-dianhydride (7CI,8CI);1,2,3,4-Cyclobutanetetracarboxylic dianhydride(6CI);Cyclobuta[1,2-c:3,4-c']difurantetrone, tetrahydro- (9CI);Cyclobutane-1,2,3,4-tetracarboxylic acid dianhydride;Cyclobutanetetracarboxylic acid dianhydride;Cyclobutanetetracarboxylicdianhydride;Maleic anhydride cyclic dimer;

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Safety information and MSDS

  • Pictogram(s):IrritantXi

  • Hazard Codes:Xi

  • 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

  • Manufacture/Brand
  • Product Description
  • Packaging
  • Price
  • Delivery
  • Purchase
  • Manufacture/Brand:Abosyn
  • Product Description:Cyclobutane-1,2,3,4-tetracarboxylic dianhydride95%-98%
  • Packaging:1g
  • Price:$ 297
  • Delivery:In stock
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  • Manufacture/Brand:AccelPharmtech
  • Product Description:1,2,3,4-Cyclobutanetetracarboxylic Dianhydride 99%
  • Packaging:10KG
  • Price:$ 1170
  • Delivery:In stock
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  • Manufacture/Brand:AccelPharmtech
  • Product Description:1,2,3,4-Cyclobutanetetracarboxylic Dianhydride 99%
  • Packaging:50G
  • Price:$ 200
  • Delivery:In stock
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  • Manufacture/Brand:Alichem
  • Product Description:Cyclobuta[1,2-c:3,4-c']difuran-1,3,4,6(3aH,3bH,6aH,6bH)-tetraone
  • Packaging:100g
  • Price:$ 457.8
  • Delivery:In stock
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  • Manufacture/Brand:Ambeed
  • Product Description:Cyclobuta[1,2-c:3,4-c']difuran-1,3,4,6(3aH,3bH,6aH,6bH)-tetraone 95%
  • Packaging:100g
  • Price:$ 435
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  • Manufacture/Brand:Ambeed
  • Product Description:Cyclobuta[1,2-c:3,4-c']difuran-1,3,4,6(3aH,3bH,6aH,6bH)-tetraone 95%
  • Packaging:25g
  • Price:$ 117
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  • Manufacture/Brand:Ambeed
  • Product Description:Cyclobuta[1,2-c:3,4-c']difuran-1,3,4,6(3aH,3bH,6aH,6bH)-tetraone 95%
  • Packaging:1g
  • Price:$ 6
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  • Manufacture/Brand:Ambeed
  • Product Description:Cyclobuta[1,2-c:3,4-c']difuran-1,3,4,6(3aH,3bH,6aH,6bH)-tetraone 95%
  • Packaging:5g
  • Price:$ 28
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  • Manufacture/Brand:Ambeed
  • Product Description:Cyclobuta[1,2-c:3,4-c']difuran-1,3,4,6(3aH,3bH,6aH,6bH)-tetraone 95%
  • Packaging:10g
  • Price:$ 53
  • Delivery:In stock
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  • Manufacture/Brand:American Custom Chemicals Corporation
  • Product Description:1,2,3,4-CYCLOBUTANETETRACARBOXYLIC DIANHYDRIDE 95.00%
  • Packaging:1G
  • Price:$ 210
  • Delivery:In stock
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Relevant articles and documentsAll total 6 Articles be found

Photodimerization of maleic anhydride in a microreactor without clogging

Horie, Tomoaki,Sumino, Motoshige,Tanaka, Takumi,Matsushita, Yoshihisa,Ichimura, Teijiro,Yoshida, Jun-Ichi

supporting information; experimental part, p. 405 - 410 (2011/03/21)

Photodimerization of maleic anhydride (MA) gives insoluble precipitated products that can be a trigger to clog a conventional microreactor. To avoid this problem, we devised a microreactor that uses liquid/gas slug flow and ultrasonication. Inert N2 gas introduced into the reaction solution swept through the reactor tube and transported precipitated products in the liquid segments.Ultrasound vibrations inhibited the adhesion and sedimentation of precipitate in the reactor tube. The combination of gas and ultrasound prevented the tube from clogging. Fluorinated ethylene propylene (FEP) tubes of various sizes were investigated to use as a tube reactor. The tubes were wound around a high-pressure Hg lamp with a Pyrex immersion well which has been using generally as a light source of photoreaction, and the reaction solution was then passed through the tube and irradiated through the tube wall. The slug flow microreactor could be operated for more than 16 h continuously without clogging. Compared to using a batch reactor, this method achieves better product quality, improved conversion, and reduced waste.

N-cyanoimides

-

, (2008/06/13)

Polyfunctional N-cyanoimides and their precursors and derivatives are disclosed along with methods for their preparation and interconversion. Also disclosed are curable compositions comprising the N-cyanoimides or poly(amide-cyanoamides) and reactive diluents as well as novel dianhydrides, polyimides, and poly(amide-cyanoamides) and methods for making them.

Development and Execution of a Production-Scale Continuous [2 + 2] Photocycloaddition

Beaver, Matthew G.,Zhang, En-Xuan,Liu, Zhi-Qing,Zheng, Song-Yuan,Wang, Bin,Lu, Jiang-Ping,Tao, Jian,Gonzalez, Miguel,Jones, Sian,Tedrow, Jason S.

, p. 2139 - 2146 (2020/06/05)

This article details the approach to large-scale production of cyclobutane 2 by the continuous-flow [2 + 2] photocycloaddition of maleic anhydride and ethylene, including (1) focused reaction optimization and development of a robust isolation protocol, (2) the approach to equipment design and process safety, and (3) the results of commissioning tests and production runs delivering the target compound at throughputs exceeding 5 kg/day.

Compounds, polymers, resin compositions and nonlinear optical devices

-

, (2008/06/13)

The present invention provides, as heteroaromatic compounds made functional so as to be used for nonlinear optical materials, compounds represented by the following general formula (1), and also provides polymers obtained from these and nonlinear optical parts comprising such polymers. In the formula, Ar1 and Ar2 each represents a divalent aromatic group; R1, R2 and R3 each represents an atom or a group independently selected from a hydrogen atom or an alkyl group and an aromatic group; X1 represents a monovalent organic group; n represents an integer of 2 to 12; and Z1 and Z2 each represents a group independently selected from electron attractive functional groups.

AROMATIC DIAMINES WITH A PHOTOREACTIVE AROMATIC SIDE GROUP, POLYAMIC ACID PHOTO-ALIGNMENT LAYERS WITH THEM AND METHOD FOR PREPARING LIQUID CRYSTAL CELLS

-

Page/Page column 27; 28, (2009/01/24)

The present invention relates to photo-alignment layers from polyamic acid with a photoreactive aromatic side group. More specifically, the present invention relates to novel polyamic acid photo-alignment layers prepared by the solution polymerization of acid dianhydrides which comprises alicyclic acid dianhydrides at certain ratio or more and aromatic diamines which comprises aromatic diamines with a photoreactive aromatic side group at certain ratio or more and the preparation method thereof, and the preparation method of aromatic diamines with novel aromatic side group. Said polyamic acid photo-alignment layers provide excellent heat- resistance, surface hardness, transparency and liquid crystal alignment property for polarized UV light.

Process route upstream and downstream products

Process route

1,2,3,4-cyclobutane tetracarboxylic acid
53159-92-5

1,2,3,4-cyclobutane tetracarboxylic acid

cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

Conditions
ConditionsYield
Withacetic anhydride; at 150 ℃; for 24h;
cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

Conditions
ConditionsYield
Bei der UV-Photolyse eines kristallinen Gemisches aus Maleinsaeure-anhydrid u. Hexamethylbenzol;
Maleinsaeureanhydrid, Photolyse in Ggw. von Aethylen in Essigester (s. Tab. II);
C6F6, /BRN= 106909/;
maleic anhydride
108-31-6

maleic anhydride

cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

Conditions
ConditionsYield
maleic anhydride;Inethyl acetate;for 240h; UV-irradiation;
Withacetic anhydride; at 150 ℃; for 24h;
Inethyl acetate;for 2h; Inert atmosphere; Slug flow microreactor; Ultrasonication; Irradiation;
2.15 g
maleic anhydride
108-31-6

maleic anhydride

ethene
74-85-1

ethene

cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

cis-1,2-cyclobutane dicarboxylic anhydride
4462-96-8

cis-1,2-cyclobutane dicarboxylic anhydride

Conditions
ConditionsYield
Withbenzophenone;Inethyl acetate;at 25 ℃; under 760.051 Torr; UV-irradiation; Flow reactor;
all-cis-Cyclobutan-tetracarbonsaeure-dianhydrid
4411-19-2,4415-87-6

all-cis-Cyclobutan-tetracarbonsaeure-dianhydrid

Conditions
ConditionsYield
Aus all-cis-Cyclobutan-tetracarbonsaeure m. Acetanhydrid b. 100grad;
Maleinsaeureanhydrid in CCl4, Photodimerisierung;
cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

C<sub>27</sub>H<sub>32</sub>BNO

C27H32BNO

C<sub>62</sub>H<sub>64</sub>B<sub>2</sub>N<sub>2</sub>O<sub>6</sub>

C62H64B2N2O6

Conditions
ConditionsYield
Withpropionic acid; at 100 - 120 ℃; for 24h; Inert atmosphere;
77%
polyamic acid

polyamic acid

cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

4-{(1E)-3-[2-(2,4-diaminophenyl)ethoxy]-3-oxoprop-1-enyl}phenyl 4-(4,4,4-trifluorobutoxy)benzoate

4-{(1E)-3-[2-(2,4-diaminophenyl)ethoxy]-3-oxoprop-1-enyl}phenyl 4-(4,4,4-trifluorobutoxy)benzoate

Conditions
ConditionsYield
cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

2,5-Dimethyl-1,4-phenylenediamine
6393-01-7

2,5-Dimethyl-1,4-phenylenediamine

2,5-bis(4-amino-2,5-dimethylphenyl)tetrahydrocyclobuta[1,2-c:3,4-c′]dipyrrole-1,3,4,6(2H,5H)tetraone

2,5-bis(4-amino-2,5-dimethylphenyl)tetrahydrocyclobuta[1,2-c:3,4-c′]dipyrrole-1,3,4,6(2H,5H)tetraone

Conditions
ConditionsYield
In1-methyl-pyrrolidin-2-one; toluene;at 180 ℃; for 9h; Inert atmosphere;
80.8%
cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

N,N'-dihydroxycyclobutanetetracarboxylic diimide
245049-70-1

N,N'-dihydroxycyclobutanetetracarboxylic diimide

Conditions
ConditionsYield
Withpyridine; hydroxylamine hydrochloride; at 20 - 90 ℃; for 0.25h;
cyclobutanetetracarboxylic dianhydride
4415-87-6

cyclobutanetetracarboxylic dianhydride

dibenzylamine
103-49-1

dibenzylamine

(1α,2β,3β,4α)-1,3-Di[N,N-dibenzylaminocarbonyl]cyclobutane-2,4-dicarboxylic acid
171348-93-9

(1α,2β,3β,4α)-1,3-Di[N,N-dibenzylaminocarbonyl]cyclobutane-2,4-dicarboxylic acid

Global suppliers and manufacturers

Global( 96) Suppliers
  • Company Name
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  • Amadis Chemical Co., Ltd.
  • Business Type:Lab/Research institutions
  • Contact Tel:86-571-89925085
  • Emails:sales@amadischem.com
  • Main Products:29
  • Country:China (Mainland)
  • Shaanxi BLOOM TECH Co.,Ltd
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-29-86470566
  • Emails:sales@bloomtechz.com
  • Main Products:80
  • Country:China (Mainland)
  • Career Henan Chemical Co
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-371-86658258
  • Emails:purchase@coreychem.com
  • Main Products:137
  • Country:China (Mainland)
  • Afine Chemicals Limited
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-571-85134551
  • Emails:info@afinechem.com
  • Main Products:92
  • Country:China (Mainland)
  • SAGECHEM LIMITED
  • Business Type:Lab/Research institutions
  • Contact Tel:+86-571-86818502
  • Emails:will@sagechem.com
  • Main Products:32
  • Country:China (Mainland)
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