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2-Pyrimidinamine, 4-methyl-, 3-oxide (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91233-73-7

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91233-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91233-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,3 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91233-73:
(7*9)+(6*1)+(5*2)+(4*3)+(3*3)+(2*7)+(1*3)=117
117 % 10 = 7
So 91233-73-7 is a valid CAS Registry Number.

91233-73-7SDS

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 2-Amino-4-methylpyrimidine 3-oxide

1.2 Other means of identification

Product number -
Other names 6-Methyl-1-oxy-pyrimidin-2-ylamine

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:91233-73-7 SDS

91233-73-7Upstream product

91233-73-7Downstream Products

91233-73-7Relevant academic research and scientific papers

Composition intended for use for retarding hair loss and for inducing and stimulating its growth, containing 2-aminopyrimidine 3-oxide derivatives, and new compounds derived from 2-aminopyrimidine 3-oxide

-

, (2008/06/13)

Composition for retarding hair loss and for inducing and stimulating its growth, containing at least one compound of formula: STR1 where R denotes H, alkyl or a ring of formula: STR2 X denotes STR3 --OR3, --SR4 with: the remaining va

Synthesis of some pyrimidine N-oxides

Jovanovic, Misa V.

, p. 1176 - 1180 (2007/10/02)

Various monosubstitudes pyrimidines and methylpyrimidines were N-oxidized with a number of different peracids.In general, they are more susceptible to side reactions accompanying N-oxidation (i.e., decomposition, annular carbon oxidation, ring opening) than other ?-deficient diazine and triazine analogs.Unsymmetrical pyrimidines, which can potentially yield two isomeric products, were N-oxidized preferentially at the site para to strong electron-donating substituents.Weaker ringactivating groups, such as methyl, are mainly ortho directing and only aid in the N-oxidation of pyrimidine nuclei having ortho/para-directing substituents.

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