38444-50-7

Basic information

• Product Name: 2,4,5-Trimethoxybenzeneacetonitrile
• Synonyms: 2,4,5-Trimethoxybenzeneacetonitrile;2,4,5-Trimethoxyphenylacetonitrile
• CAS NO: 38444-50-7
• Molecular Formula: C₁₁H₁₃NO₃
• Molecular Weight: 207.23
• Mol File: 38444-50-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 85 °C
• Boiling Point: 337.2±37.0 °C(Predicted)
• Appearance: /
• Density: 1.104±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2,4,5-Trimethoxybenzeneacetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,5-Trimethoxybenzeneacetonitrile(38444-50-7)
• EPA Substance Registry System: 2,4,5-Trimethoxybenzeneacetonitrile(38444-50-7)

Safety Data

• Hazardous Substances Data: 38444-50-7(Hazardous Substances Data)

Upstream product

• 53811-44-2 2,4,5-trimethoxybenzyl chloride 
• 143-33-9 sodium cyanide 
• 490-64-2 asaronic acid 
• 30038-31-4 (2,4,5-trimethoxyphenyl)methanol 
• 50-00-0 formaldehyd 
• 4460-86-0 asaraldehyde 
• 151-50-8 potassium cyanide 
• 38449-36-4 (2,4,5-trimethoxy-phenyl)-pyruvic acid 
• 20029-76-9 methyl 2,4,5-trimethoxybenzoate 

Downstream Products

• 72545-40-5 2',4',6'-trihydroxy-(2,4,5-trimethoxyphenyl)acetophenone 
• 4463-16-5 2,4,5-trimethoxyphenylacetic acid 
• 854866-54-9 4-dimethylamino-2-(2,4,5-trimethoxy-phenyl)-butyronitrile 
• 6468-53-7 2-hydroxy-2',4,4',5',6-pentamethoxybenzoin 
• 15394-83-9 1-(2,4,5-trimethoxyphenyl)-2-aminoethane 
• 60059-04-3 2-Methyl-2-(2,4,5-trimethoxy-phenyl)-propionitrile 
• 58084-83-6 2',4',5,5'-tetramethoxy-2,2-dimethylpyrano<5,6-g>isoflavone 
• 1446307-19-2 C₂₂H₁₈O₇ 
• 75340-02-2 5,7-dihydroxy-3-(2,4,5-trimethoxyphenyl)chromen-4-one 
• 1446307-18-1 7-(1,1-dimethylpropargyloxy)-5-hydroxy-2',4',5'-trimethoxyisoflavone 
• 58084-82-5 C₂₃H₂₂O₇ 
• 3044-60-8 5-hydroxy-2',4',5'-trimethoxy-2,2-dimethylpyrano<6,5-h>isoflavone 
• 1199-18-4 6-Hydroxydopamin 
• 122315-51-9 4-acetoxy-5,7-dimethoxy-3-(2,4,5-trimethoxy-phenyl)-coumarin 

Relevant articles and documents

Studies on the total synthesis of Hirtellanine A: Regioselective synthesis of benzopyran

The total synthesis of Hirtellanine A was accomplished by two different synthetic approaches. Hirtellanine A was assembled using a one-pot, tandem acid-mediated deprotection and tautomerization cascade starting from quinone derivative 23. The key features

Chemical Transformation of Protoberberines. Part 10. A Novel Synthesis of Sanguilutine and Dihydrosanguilutine, fully Aromatised 2,3,7,8,10-Pentaoxygenated Benzophenanthridine Alkaloids

2,3,7,8,10-Pentaoxygenated benzophenanthridine alkaloids, sanguilutine (1) and dihydrosanguilutine (2), were efficiently synthesized from the corresponding 2,3,9,10,12-pentamethoxyprotoberberine (8) through a regioselective C(6)-N bond cleavage, followed by recombination between the original C(6) and C(13) positions of compound (8) according to a biomimetic route.