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38499-22-8

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38499-22-8 Usage

General Description

3-AMINO-3-(4-ETHOXYPHENYL)PROPANOIC ACID, also known as ethyl 3-amino-3-(4-ethoxyphenyl)propanoate, is a chemical compound with a molecular formula C11H17NO3. It is an amino acid derivative with a propanoic acid backbone, and a 4-ethoxyphenyl group attached to the alpha carbon. 3-AMINO-3-(4-ETHOXYPHENYL)PROPANOIC ACID is often used as a synthetic intermediate in the production of pharmaceuticals and other organic compounds. It has potential applications in medicinal chemistry, particularly in the development of drugs targeting specific biological pathways. Despite its potential utility in chemical synthesis, it is important to handle this compound with caution, as it may pose health and safety risks if not properly handled and used.

Check Digit Verification of cas no

The CAS Registry Mumber 38499-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,9 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38499-22:
(7*3)+(6*8)+(5*4)+(4*9)+(3*9)+(2*2)+(1*2)=158
158 % 10 = 8
So 38499-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c1-2-15-9-5-3-8(4-6-9)10(12)7-11(13)14/h3-6,10H,2,7,12H2,1H3,(H,13,14)

38499-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-AMINO-3-(4-ETHOXYPHENYL)PROPANOIC ACID

1.2 Other means of identification

Product number -
Other names 3-Amino-3-(4-ethoxy-phenyl)-propionic 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:38499-22-8 SDS

38499-22-8Downstream Products

38499-22-8Relevant articles and documents

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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