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(R)-3-Amino-3-(3,5-dimethyl)-propionic acid is an organic compound with the molecular formula C7H15NO2, derived from the amino acid valine and featuring an additional methyl group on the side chain. This chiral compound is characterized by its specific (R)conformation, making it a significant building block in organic synthesis and pharmaceutical research for the development of new drugs and pharmaceuticals with potential therapeutic applications.

792183-19-8

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792183-19-8 Usage

Uses

Used in Pharmaceutical Research:
(R)-3-Amino-3-(3,5-dimethyl)-propionic acid is used as a starting material in pharmaceutical research for the production of various drugs and pharmaceuticals. Its unique properties and structure contribute to the creation of new compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-3-Amino-3-(3,5-dimethyl)-propionic acid serves as a valuable building block, enabling the development of novel compounds with specific functions and properties, which can be further utilized in various chemical and pharmaceutical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 792183-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,1,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 792183-19:
(8*7)+(7*9)+(6*2)+(5*1)+(4*8)+(3*3)+(2*1)+(1*9)=188
188 % 10 = 8
So 792183-19-8 is a valid CAS Registry Number.

792183-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-amino-3-(3,5-dimethoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names (R)-3-Amino-3-(3,5-dimethoxyphenyl)propanoic acid

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:792183-19-8 SDS

792183-19-8Downstream Products

792183-19-8Relevant academic research and scientific papers

Parallel synthesis of homochiral β-amino acids

Davies, Stephen G.,Mulvaney, Andrew W.,Russell, Angela J.,Smith, Andrew D.

, p. 1554 - 1566 (2008/02/09)

The parallel asymmetric synthesis of an array of 30 β-amino acids of high enantiomeric purity using the conjugate addition of homochiral lithium N-benzyl-N-(α-methylbenzyl)amide as the key step is accomplished. The experimental simplicity and highly practical nature of the protocol is demonstrated by the efficient parallel conversion of 15 α,β-unsaturated esters to both enantiomeric series of the corresponding β-amino acids in high overall yields and selectivities with minimal purification involved in each step of the reaction protocol.

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