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(R)-3-(3-Phenoxyphenyl)-beta-alanine, a chiral molecule with the molecular formula C16H16NO3, is a beta-alanine derivative and a non-essential amino acid that functions as a neurotransmitter in the brain. The (R)-enantiomer represents the specific stereochemistry of (R)-3-(3-PHENOXYPHENYL)-BETA-ALANINE, which is a potential building block for the synthesis of pharmaceuticals or other bioactive molecules due to its unique structure and properties. It may also have potential applications in the development of new drugs or in chemical research.

715653-77-3

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715653-77-3 Usage

Uses

Used in Pharmaceutical Industry:
(R)-3-(3-Phenoxyphenyl)-beta-alanine is used as a building block for the synthesis of pharmaceuticals or other bioactive molecules, leveraging its unique structure and properties to create new drugs or enhance existing ones.
Used in Chemical Research:
(R)-3-(3-Phenoxyphenyl)-beta-alanine is utilized in chemical research to explore its potential applications and properties, contributing to the advancement of scientific knowledge and the development of innovative compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 715653-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,5,6,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 715653-77:
(8*7)+(7*1)+(6*5)+(5*6)+(4*5)+(3*3)+(2*7)+(1*7)=173
173 % 10 = 3
So 715653-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H15NO3/c16-14(10-15(17)18)11-5-4-8-13(9-11)19-12-6-2-1-3-7-12/h1-9,14H,10,16H2,(H,17,18)/t14-/m1/s1

715653-77-3SDS

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 (R)-3-amino-3-(3-phenoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names -

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:715653-77-3 SDS

715653-77-3Downstream Products

715653-77-3Relevant academic research and scientific papers

ANTAGONISTS OF HUMAN INTEGRIN (ALPHA4)(BETA7)

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Paragraph 0228; 0418; 0419, (2019/10/29)

Disclosed are small molecule antagonists of α4β7 integrin, and methods of using them to treat a number of specific diseases or conditions.

Propionic Acid Derivatives and Methods of Use Thereof

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Paragraph 0387; 0388, (2018/11/21)

Provided herein are compounds and pharmaceutical compositions of formula I where R1, R2, R3, R4, R5, X and R6 are as described herein. Also provided pharmaceutically acceptable salts or stereoisomer(s) of these compounds. In addition methods are provided for antagonizing the action of an α4-integrin to treat various pathophysiological conditions.

Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium

Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov

, p. 1113 - 1124 (2007/10/03)

The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.

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