690639-23-7

Basic information

• Product Name: 2-Propenoic acid, 2-azido-3-(3,4-dimethoxyphenyl)-, methyl ester
• CAS NO: 690639-23-7
• Molecular Formula: C12H13N3O4
• Molecular Weight: 263.253
• Mol File: 690639-23-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 2-azido-3-(3,4-dimethoxyphenyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 2-azido-3-(3,4-dimethoxyphenyl)-, methyl ester(690639-23-7)
• EPA Substance Registry System: 2-Propenoic acid, 2-azido-3-(3,4-dimethoxyphenyl)-, methyl ester(690639-23-7)

Safety Data

• Hazardous Substances Data: 690639-23-7(Hazardous Substances Data)

Usage

Chemical compound

2-Propenoic acid, 2-azido-3-(3,4-dimethoxyphenyl)-, methyl ester

Also known as

Azidomethyl ester of ferulic acid

Derivative of ferulic acid

A common component of plant cell walls and an antioxidant with potential health benefits

Azido group

Makes it useful for bioconjugation applications

Methyl ester form

Allows for better solubility and stability in organic solvents

Versatile compound

Suitable for various research and industrial purposes in chemical and biological applications

Upstream product

• 1816-92-8 Methyl azidoacetate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 54814-41-4 (+/-)-(R)-methyl 3-(3,4-dimethoxyphenyl)-2-hydroxypropanoate 
• 54814-41-4 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester 
• 153381-08-9 Methyl (S)-(+)-3-(3,4 dimethoxyphenyl)-2-hydroxypropionate 
• 28059-24-7 methyl 5,6-dimethoxy-1H-indole-2-carboxylate 
• 157670-11-6 (R)-6,7-Dimethoxy-1-methyl-2-((S)-1-phenyl-ethyl)-2,3,4,9-tetrahydro-1H-β-carboline 
• 157670-09-2 2-(5,6-Dimethoxy-1H-indol-3-yl)-2-oxo-N-((S)-1-phenyl-ethyl)-acetamide 
• 157670-10-5 [2-(5,6-Dimethoxy-1H-indol-3-yl)-ethyl]-((S)-1-phenyl-ethyl)-amine 
• 14430-23-0 5,6-dimethoxyindole 
• 88210-96-2 5,6-dimethoxyindole-2-carboxylic acid 

Relevant articles and documents

Synthesis of symmetrical and unsymmetrical diindolylmethanes via acid-catalysed electrophilic substitution reactions

A range of activated indole-2-carboxylate derivatives was prepared via the Hemetsberger indole synthesis. Vilsmeier formylation was explored to establish regioselectivity and to prepare a range of new indole carbaldehydes. The indole aldehydes were reduce

The synthesis of roeharmine and (-)-1,2,3,4-tetrahydroroeharmine

The total synthesis of roeharmine 1 as well as an enantiospecific synthesis of (-)-1,2,3,4-tetrahydroroeharmine 2 has been achieved via the Pictet-Spengler reaction as a key step. The optical rotation of synthetic (- )-2 was found to be higher than that reported for the natural product. A possible mechanism for the racemization of 2 upon exposure to acid has been proposed and serves as a warning to alkaloid chemists who isolate ring-A alkoxylated indole alkaloids under acidic conditions.