183509-48-0

Basic information

• Product Name: (R)-2-BENZYLBUT-3-ENOIC ACID
• Synonyms: (R)-2-BENZYLBUT-3-ENOIC ACID
• CAS NO: 183509-48-0
• Molecular Formula: C₁₁H₁₂O₂
• Molecular Weight: 176.21
• Mol File: 183509-48-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-2-BENZYLBUT-3-ENOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-BENZYLBUT-3-ENOIC ACID(183509-48-0)
• EPA Substance Registry System: (R)-2-BENZYLBUT-3-ENOIC ACID(183509-48-0)

Safety Data

• Hazardous Substances Data: 183509-48-0(Hazardous Substances Data)

Usage

Description

(R)-2-BENZYLBUT-3-ENOIC ACID, with the molecular formula C12H14O2, is an organic compound that is chiral, meaning it has a non-superimposable mirror image. The (R)designation indicates its specific stereochemistry. (R)-2-BENZYLBUT-3-ENOIC ACID is known for its characteristic sweet, floral aroma and is valued in various industries due to its diverse applications.

Uses

Used in Pharmaceutical Synthesis:
(R)-2-BENZYLBUT-3-ENOIC ACID is used as a key intermediate in the pharmaceutical industry for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medications.
Used in Fragrance and Flavor Production:
(R)-2-BENZYLBUT-3-ENOIC ACID is used as a component in the fragrance and flavor industry due to its distinct sweet, floral aroma. This property makes it a desirable ingredient in the creation of perfumes, colognes, and a variety of flavorings for the food and beverage sector.
Used in Organic Chemistry:
(R)-2-BENZYLBUT-3-ENOIC ACID serves as a precursor for the creation of other important organic molecules in the field of organic chemistry. Its versatility and unique properties contribute to the synthesis of a wide range of compounds with various applications in different industries.

Upstream product

• 110036-21-0 2-benzylbut-3-enenitrile 
• 100-39-0 benzyl bromide 
• 127392-99-8 N-[(2R)-2-benzyl-3-butenoyl]-(1S)-2,10-camphorsultam 

Downstream Products

• 484051-36-7 (2R,1'R)-N-(1'-benzyl-prop-2'-enyl)-N-[(2,4-dimethoxyphenyl)methyl]-2-benzyl-but-3-enamide 
• 484051-40-3 (3R,6R)-N-[(2,4-dimethoxyphenyl)methyl]-3,6-dibenzyl-3,6-dihydro-2-pyridone 
• 484051-51-6 (3R,6R)-3,6-dibenzyl-2-ethoxy-3,6-dihydropyridine 
• 214072-07-8 (3R,6R)-3,6-dibenzyl-3,6-dihydro-2-pyridone 
• 332424-94-9 (3R,6S)-3,6-Dibenzyl-2-ethoxy-3,6-dihydropyridine 
• 214072-06-7 (3R,6S)-3,6-dibenzyl-3,6-dihydro-1H-pyridin-2-one 
• 214072-04-5 (2R,1'S)-N-(1'-benzyl-prop-2'-enyl)-N-[(2,4-dimethoxyphenyl)methyl]-2-benzyl-but-3-enamide 
• 214072-05-6 (3R,6S)-N-[(2,4-Dimethoxyphenyl)methyl]-3,6-dibenzyl-3,6-dihydro-2-pyridone 
• 866994-30-1 (2S,3S)-2-benzyl-3-fluoropent-4-enoic acid 
• 866994-27-6 (2S,3R)-2-benzyl-3-fluoropent-4-enoic acid 
• 866994-24-3 (2R)-2-benzyl-5-(trimethylsilyl)pent-3-enoic acid 
• 214072-03-4 (2R)-2-benzyl-3-butenoyl chloride 

Relevant articles and documents

Remarkable electronic and steric effects in the nitrile biotransformations for the preparation of enantiopure functionalized carboxylic acids and amides: Implication for an unsaturated carbon-carbon bond binding domain of the amidase

(Chemical Equation Presented) Biotransformations of various functionalized racemic nitriles catalyzed by Rhodococcus erythropolis AJ270, a nitrile hydratase/amidase-containing microbial whole-cell catalyst, were studied. While the nitrile hydratase exhibi

Enantioconservative synthesis and ring closing metathesis of disubstituted dialkenic amides

Optically pure disubstituted dialkenic amides 2, which are direct precursors of Z-ethylenic pseudo-peptides 1, are readily synthesized and then cyclized to lactams 3 in the presence of Grubbs' ruthenium-based metathesis catalysts with total conservation of enantiomeric purity.