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14080-19-4

14080-19-4

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14080-19-4 Usage

Chemical Properties

Light yellow to brown liquid

Check Digit Verification of cas no

The CAS Registry Mumber 14080-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,8 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14080-19:
(7*1)+(6*4)+(5*0)+(4*8)+(3*0)+(2*1)+(1*9)=74
74 % 10 = 4
So 14080-19-4 is a valid CAS Registry Number.

14080-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Methylsulfinyl)pyrimidine

1.2 Other means of identification

Product number -
Other names Ethanol,2-(methylsulfinyl)-,acetate

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:14080-19-4 SDS

14080-19-4Downstream Products

14080-19-4Relevant articles and documents

Comparative study of metal-catalyzed iminations of sulfoxides and sulfides

Mancheno, Olga Garcia,Bolm, Carsten

, p. 6674 - 6681 (2008/03/15)

A comparative study of the imination of sulfur compounds with various metal catalysts in combination with isolated or in situ generated iminoiodinanes (PhI=NR) as nitrogen sources is presented. The influence of the metal catalyst towards the imination of a variety of substituted sulfoxides has been evaluated. Moreover, the effect of the different oxidation states of sulfur on the reactivity and selectivity of the nitrogen transfer redox process in the formation of sulfilimines and sulfoximines was studied. Depending on both the specific metal catalyst as well as the employed nitrene precursor, the sulfide/sulfoxide imination ratio varied in transformations of thianthrene-5-oxide and substituted para-thio phenylsulfoxides.

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