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183509-48-0

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183509-48-0 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.

Check Digit Verification of cas no

The CAS Registry Mumber 183509-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,5,0 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 183509-48:
(8*1)+(7*8)+(6*3)+(5*5)+(4*0)+(3*9)+(2*4)+(1*8)=150
150 % 10 = 0
So 183509-48-0 is a valid CAS Registry Number.

183509-48-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Benzyl-3-butenoic acid

1.2 Other means of identification

Product number -
Other names D-norvaline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:183509-48-0 SDS

183509-48-0Relevant 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

Gao, Ming,Wang, De-Xian,Zheng, Qi-Yu,Huang, Zhi-Tang,Wang, Mei-Xiang

, p. 6060 - 6066 (2008/02/10)

(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

Sauriat-Dorizon, Helene,Guibe, Francois

, p. 6711 - 6714 (2007/10/03)

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.

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