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3-(3-Hydroxyphenyl)-DL-beta-alanine, also known as beta-(3-Hydroxyphenyl)-DL-alanine, is a synthetic compound that is a derivative of beta-alanine. It is structurally related to beta-alanine, a naturally occurring beta-amino acid that is primarily used by the body to produce carnosine and other biochemically important molecules like pantothenic acid (vitamin B5). The phenolic hydroxyl group in 3-(3-Hydroxyphenyl)-DL-beta-alanine, which is a functional group consisting of a central carbon atom attached to three oxygen atoms, indicates the presence of a hydroxy group which can significantly alter its physical characteristics and its bioactivity. It is a less common chemical that can play an intermediate role in various synthetic and metabolic chemical reactions. However, more research is required to fully understand its potential uses and biochemical functions.

102872-33-3

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102872-33-3 Usage

Uses

Used in Pharmaceutical Industry:
3-(3-Hydroxyphenyl)-DL-beta-alanine is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure and bioactivity make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Cosmetic Industry:
3-(3-Hydroxyphenyl)-DL-beta-alanine is used as an active ingredient in cosmetic formulations for its potential skin care benefits. The phenolic hydroxyl group may contribute to antioxidant properties, which can help protect the skin from oxidative stress and promote overall skin health.
Used in Research and Development:
3-(3-Hydroxyphenyl)-DL-beta-alanine is used as a research compound in various scientific studies to explore its potential applications and understand its biochemical functions. This can lead to the discovery of new uses and applications in different industries, such as pharmaceuticals, cosmetics, and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 102872-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,7 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102872-33:
(8*1)+(7*0)+(6*2)+(5*8)+(4*7)+(3*2)+(2*3)+(1*3)=103
103 % 10 = 3
So 102872-33-3 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)

102872-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-2-(3-hydroxyphenyl)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:102872-33-3 SDS

102872-33-3Downstream Products

102872-33-3Relevant academic research and scientific papers

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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