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N-(2-hydroxybenzyl)-N-methylhydrazine, also known as NSC 93, is an organic compound with the chemical formula C8H12N2O. It is a derivative of hydrazine, featuring a benzyl group attached to the nitrogen atom, with a hydroxyl group on the benzene ring and a methyl group on the other nitrogen atom. N-(2-hydroxybenzyl)-N-methylhydrazine has been studied for its potential antitumor properties and is used in scientific research to investigate various biological processes. It is important to note that hydrazine and its derivatives can be toxic and require careful handling.

5638-98-2

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5638-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5638-98-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5638-98:
(6*5)+(5*6)+(4*3)+(3*8)+(2*9)+(1*8)=122
122 % 10 = 2
So 5638-98-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O/c1-10(9)6-7-4-2-3-5-8(7)11/h2-5,11H,6,9H2,1H3

5638-98-2SDS

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-[[amino(methyl)amino]methyl]phenol

1.2 Other means of identification

Product number -
Other names Nsd 1039

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 -
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More Details:5638-98-2 SDS

5638-98-2Relevant academic research and scientific papers

Exploiting neighboring-group interactions for the self-selection of a catalytic unit

Gasparini, Giulio,Prins, Leonard J.,Scrimin, Paolo

supporting information; experimental part, p. 2475 - 2479 (2009/02/06)

(Figure Presented) A good neighbor is better than a far-away friend: A tethering strategy is used to self-select groups that assist in the cleavage of a neighboring carboxylic ester moiety (see picture, TSA=transition-state analogue). A correlation is observed between the amplification at thermodynamic equilibrium and the catalytic efficiency.

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