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CAS No.: | 34374-88-4 |
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Name: | 1,3,5-Benzenetricarboxaldehyde, 2,4,6-trihydroxy- |
Article Data: | 55 |
Cas Database | |
Molecular Structure: | |
Formula: | C9H6O6 |
Molecular Weight: | 210.143 |
Synonyms: | 2,4,6-Trihydroxytrimesinaldehyd;1,3,5-triformylphoroglucinol;2,4,6-triformylphloroglucinol;2,4,6-trihydroxybenzene-1,3,5-tricarbaldehyde;2,4,6-trihydroxy-1,3,5-benzenetricarbaldehyde;triformylphloroglucinol; |
EINECS: | N/A |
Density: | 1.72 g/cm3 |
Melting Point: | 198 - 200 °C |
Boiling Point: | N/A |
Flash Point: | N/A |
Solubility: | N/A |
Appearance: | White to yellow solid |
Hazard Symbols: | N/A |
Risk Codes: | N/A |
Safety: | |
Transport Information: | N/A |
PSA: | 111.90000 |
LogP: | 0.24090 |
2,4-diformyl 2,4,6-trihydroxybenzene
trifluoroacetic acid
2,4,6-triformylphloroglucinol
Conditions | Yield |
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Stage #1: 2,4-diformyl 2,4,6-trihydroxybenzene With hexamethylenetetramine at 60℃; for 1.5h; Schlenk technique; Stage #2: trifluoroacetic acid at 100℃; for 4h; Inert atmosphere; Schlenk technique; Stage #3: With hydrogenchloride In water at 100℃; for 1h; Inert atmosphere; Schlenk technique; | 60% |
Conditions | Yield |
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Stage #1: 3,5-dihydroxyphenol; formamidine acetic acid With acetic anhydride In tetrahydrofuran at 45℃; for 24h; Sealed tube; Stage #2: With water; lithium hydroxide for 18h; | 51% |
Conditions | Yield |
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Stage #1: 3,5-dihydroxyphenol; hexamethylenetetramine With trifluoroacetic acid at 100℃; for 2h; Inert atmosphere; Stage #2: With hydrogenchloride; water at 100℃; for 2h; | 23% |
Stage #1: 3,5-dihydroxyphenol; hexamethylenetetramine With trifluoroacetic acid at 100℃; for 5h; Duff Aldehyde Synthesis; Stage #2: With hydrogenchloride In water at 100℃; Duff Aldehyde Synthesis; | 22% |
Stage #1: 3,5-dihydroxyphenol; hexamethylenetetramine With trifluoroacetic acid at 100℃; for 2.5h; Inert atmosphere; Stage #2: With hydrogenchloride; water for 1h; Inert atmosphere; | 22% |
Conditions | Yield |
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Stage #1: 3,5-dihydroxyphenol; hexamine With trifluoroacetic acid at 100℃; for 5h; Duff reaction; Stage #2: With hydrogenchloride In water at 100℃; for 1h; | 22% |
Conditions | Yield |
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With hexamethylenetetramine at 100℃; for 0.2h; Inert atmosphere; | 22% |
Stage #1: 3,5-dihydroxyphenol; trifluoroacetic acid With hexamethylenetetramine for 2h; Reflux; Stage #2: With hydrogenchloride In water for 1.5h; Reflux; | 20% |
Stage #1: 3,5-dihydroxyphenol; trifluoroacetic acid With hexamethylenetetramine for 2h; Reflux; Stage #2: With hydrogenchloride In water for 1.5h; | |
With hexamethylenetetramine | |
Stage #1: 3,5-dihydroxyphenol; trifluoroacetic acid With hexamethylenetetramine at 100℃; for 3h; Reflux; Inert atmosphere; Stage #2: With hydrogenchloride In water at 100℃; for 1h; Inert atmosphere; |
2-(3-tert-butyldimethylsilyloxyl-1-propynyl)-4-tert-butylaniline
2,4,6-triformylphloroglucinol
Conditions | Yield |
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In ethanol at 90℃; | 99% |
(S)-3-(2-amino-5-tert-butylphenyl)-1-phenylprop-2-yn-1-ol
2,4,6-triformylphloroglucinol
(2E,4E,6E)-2,4,6-tris((4-tert-butyl-2-((S)-3-hydroxy-3-phenylprop-1-ynyl)phenylamino)methylene)cyclohexane-1,3,5-trione
Conditions | Yield |
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In ethanol at 20℃; Reflux; | 99% |
(1S,1'S)-3,3'-(2-amino-5-tert-butyl-1,3-phenylene)bis(1-phenyl-prop-2-yn-1-ol)
2,4,6-triformylphloroglucinol
(2E,4E,6E)-2,4,6-tris((4-tert-butyl-2,6-bis((S)-3-hydroxy-3-phenylprop-1-ynyl)phenylamino)methylene)cyclohexane-1,3,5-trione
Conditions | Yield |
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In ethanol at 20℃; Reflux; | 99% |
aminoferrocene
2,4,6-triformylphloroglucinol
Conditions | Yield |
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In ethanol soln. of Fe complex and C6(OH)3(CHO)3 in EtOH refluxed for 24 h; cooled to room temp.; filtered; ppt. washed with Et2O; dried under vac.; mixt. of two isomers obtained; | 99% |
Conditions | Yield |
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Stage #1: N,N-dimethylammonium chloride With 1,8-diazabicyclo[5.4.0]undec-7-ene Schlenk technique; Inert atmosphere; Sonication; Stage #2: 2,4,6-triformylphloroglucinol In chloroform-d1 at 20℃; Inert atmosphere; | 99% |