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N-benzyl-N-methylglycine, also known as benzylmethylglycine, is a glycine derivative chemical compound that features a benzyl group and a methylglycine group. It is recognized for its potential therapeutic applications and is widely utilized in organic synthesis and pharmaceutical research due to its ability to modulate neurotransmitter function and inhibit protein kinase C. As a free form molecular entity, its properties and uses are well-documented in chemical databases.

37429-48-4

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37429-48-4 Usage

Uses

Used in Pharmaceutical Research and Organic Synthesis:
N-benzyl-N-methylglycine(SALTDATA: FREE) is used as a building block for its role in the development of pharmaceutical drugs and as a reagent in various chemical reactions, contributing to the advancement of both fields.
Used in Therapeutic Applications:
In the medical and pharmaceutical industry, N-benzyl-N-methylglycine(SALTDATA: FREE) is used as a modulator of neurotransmitter function, which is crucial for influencing biological processes. Its ability to inhibit protein kinase C also makes it a candidate for the treatment of various conditions where such inhibition can be beneficial.
Used in the Production of Pharmaceutical Drugs:
N-benzyl-N-methylglycine(SALTDATA: FREE) serves as a key component in the manufacturing process of certain pharmaceutical drugs, highlighting its importance in the development of new medications and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 37429-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37429-48:
(7*3)+(6*7)+(5*4)+(4*2)+(3*9)+(2*4)+(1*8)=134
134 % 10 = 4
So 37429-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-11(8-10(12)13)7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3,(H,12,13)

37429-48-4SDS

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 2-[benzyl(methyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-methyl-glycin

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:37429-48-4 SDS

37429-48-4Relevant academic research and scientific papers

Hepatitis C Virus Inhibitors

-

Page/Page column 47, (2008/06/13)

The present disclosure relates to compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.

Herbicidal imidazole-5-carboxylic acid derivatives

-

, (2008/06/13)

A method for controlling weeds preferably in the crops of useful plants by using a 1-methyl-1H-imidazole-5-carboxylic acid derivative; herbicidal compositions containing the same; 1-methyl-1H-imidazole-5-carboxylic acid derivatives.

N-OXIDES OF N-METHYL-N-BENZYL-α-AMINO ACIDS. SYNTHESIS AND SPECTROSCOPIC PROPERTIES

Marks, Krystyna,Siemion, Ignacy Z.,Sucharda-Sobczyk, Anna

, p. 109 - 121 (2007/10/02)

A method of synthesizing chiral N-methyl-N-benzylamino acid N-oxides has been elaborated.For the resolved diastereoisomeric N-oxides 1H NMR, IR, UV and CD spectra were recorded.The problem of configuration on the chiral nitrogen atoms and asymmetric induction during the synthesis has been discussed.

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