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26049-12-7

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26049-12-7 Usage

General Description

3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is a chemical compound that consists of a 3-amino-3-(3-hydroxyphenyl)propionic acid molecule. It is a derivative of phenylalanine and belongs to the class of organic compounds known as phenylpropanoic acids. 3-AMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is commonly used as a chiral building block in the synthesis of pharmaceuticals, especially those with potential analgesic and anti-inflammatory properties. The hydroxyl group and amino group in the molecule make it a versatile intermediate in organic chemistry, allowing for its use in the creation of diverse chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 26049-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,4 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26049-12:
(7*2)+(6*6)+(5*0)+(4*4)+(3*9)+(2*1)+(1*2)=97
97 % 10 = 7
So 26049-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c10-8(5-9(12)13)6-2-1-3-7(11)4-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m1/s1

26049-12-7SDS

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 3-Amino-3-(3-hydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names DL--(3-Hydroxyphenyl)alanine

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:26049-12-7 SDS

26049-12-7Downstream Products

26049-12-7Relevant articles and documents

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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