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21384-43-0

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21384-43-0 Usage

General Description

(2-methylaziridin-1-yl)(3-methylphenyl)methanone is a chemical compound also known as "methaziridine." It is a synthetic organic compound that consists of a five-membered aziridine ring with a methyl group and a phenyl group attached to it. Methaziridine is primarily used in organic synthesis as a reagent for the formation of heterocyclic compounds and as a precursor in the production of various pharmaceuticals and agrochemicals. It is also used in the manufacture of dyes, pigments, and other specialty chemicals. Methaziridine is considered to be a potentially hazardous chemical and should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 21384-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,8 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21384-43:
(7*2)+(6*1)+(5*3)+(4*8)+(3*4)+(2*4)+(1*3)=90
90 % 10 = 0
So 21384-43-0 is a valid CAS Registry Number.

21384-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylaziridin-1-yl)-(3-methylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2-Methyl-1-m-toluyl-aziridin

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:21384-43-0 SDS

21384-43-0Relevant articles and documents

Synthesis and biological activities of 4-phenyl-5-pyridyl-1,3-thiazole derivatives as selective adenosine A3 antagonists

Miwatashi, Seiji,Arikawa, Yasuyoshi,Matsumoto, Tatsumi,Uga, Keiko,Kanzaki, Naoyuki,Imai, Yumi N.,Ohkawa, Shigenori

experimental part, p. 1126 - 1137 (2009/09/25)

To investigate the potency of an adenosine A3 receptor (A 3AR) antagonist as an anti-asthmatic drug, a novel series of 4-phenyl-5-pyridyl-1,3-thiazole derivatives was synthesized and evaluated in human adenosine A1, A

JNK INHIBITOR

-

Page/Page column 79, (2010/02/07)

The present invention relates to a c-Jun N-terminal kinase inhibitor containing an azole compound (I) substituted by a nitrogen-containing aromatic group having substituent(s)(except a compound represented by the formula: ) or a salt thereof or a prodrug thereof.

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