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4401-12-1

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4401-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4401-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4401-12:
(6*4)+(5*4)+(4*0)+(3*1)+(2*1)+(1*2)=51
51 % 10 = 1
So 4401-12-1 is a valid CAS Registry Number.

4401-12-1SDS

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 trans-1-(3-methyloxiranyl)-ethanone

1.2 Other means of identification

Product number -
Other names trans-3-methyl-2-acetyloxirane

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:4401-12-1 SDS

4401-12-1Relevant articles and documents

SYNTHESIS OF 2-ALKYLTHIO-5-ACETYL-2-OXAZOLINES

Bubel', O.N.,Tishchenko, I.G.,Grinkevich, O.A.,Abramov, A.F.

, p. 352 - 355 (1980)

The reaction of 2-acetyloxiranes with alkyl thiocyanates in the presence of Lewis acids (BF3, AlCl3) has given 2-alkylthio-5-acetyl-2-oxazolines (yields 40-60percent).It has been shown that the reaction of trans-2-acetyl-3-methyloxirane and of trans-2-acetyl-3-methyloxirane and of trans-2-acetyl-2,3-dimethyloxirane with alkyl thiocyanates takes place stereospecifically and leads to cis-2-alkylthio-5-acetyl-2-oxazolines.

FORMATION OF α,β-EPOXY SYSTEMS FROM β-PEROXY CARBON FREE RADICALS

Corey, E. J.,Schmidt Greg,Shimoji Katsuichi

, p. 3169 - 3170 (2007/10/02)

The conversion of β-peroxy carbon free radicals to α,β-epoxides is a facile process of broad scope and may be a key step in the biosynthesis of clavulones.

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