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149692-49-9

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149692-49-9 Usage

General Description

3-[benzyl(methyl)amino]propanoic acid, also known as benzyldimethylaminoacetic acid, is a compound that belongs to the class of amino acids. It is a derivative of propanoic acid with a benzyl group attached to the amino group at the third position. This chemical is often used in the synthesis of pharmaceuticals and as a reagent in organic chemistry. The benzyl and methyl groups provide this compound with unique properties and make it useful in various chemical processes. However, it is important to handle this chemical with care due to its potential hazards and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 149692-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,6,9 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 149692-49:
(8*1)+(7*4)+(6*9)+(5*6)+(4*9)+(3*2)+(2*4)+(1*9)=179
179 % 10 = 9
So 149692-49-9 is a valid CAS Registry Number.

149692-49-9SDS

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 N-Benzyl-N-methyl-β-alanine

1.2 Other means of identification

Product number -
Other names 3-(benzyl(methyl)amino)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:149692-49-9 SDS

149692-49-9Relevant articles and documents

Synthesis method of 3-methylaminopropionic acid

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Paragraph 0008, (2021/01/24)

The invention relates to a synthetic method of 3-methylaminopropionic acid. The method mainly solves the technical problems that the existing method for preparing 3-methylaminopropionic acid has manyreaction steps and is not easy for large-scale productio

ARYLOXY-AND HETEROARYLOXY-SUBSTITUTED TETRAHYDROBENZAZEPINES AND USE THEREOF TO BLOCK REUPTAKE OF NOREPINEPHRINE, DOPAMINE, AND SEROTONIN

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Page/Page column 87, (2009/01/20)

The aryloxy- and heteroaryloxy-substituted tetrahydrobenzazepine derivative compounds of the present invention are represented by formulae (I) (A-E) having the following structure where the carbon atom designated * is in the R or S configuration and the s

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