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40289-98-3

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40289-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40289-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,8 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40289-98:
(7*4)+(6*0)+(5*2)+(4*8)+(3*9)+(2*9)+(1*8)=123
123 % 10 = 3
So 40289-98-3 is a valid CAS Registry Number.

40289-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylsulfanyloctadecane

1.2 Other means of identification

Product number -
Other names methyl octadecyl sulphide

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:40289-98-3 SDS

40289-98-3Relevant articles and documents

Copper-catalyzed thiocarbonylation and thiolation of alkyl iodides

Tian, Qingqiang,Sun, Rongjing,Li, Yahui

supporting information, p. 1186 - 1190 (2022/02/19)

In the present study, an efficient Cu-catalyzed transthiolation of alkyl iodides is developed. Notably, in the presence of CO, thioesters could also be obtained with copper and cobalt as the co-catalyst. This transformation displayed good functional group

Hydrozirconation of oleyl sulphides and oleyl phenylsulphone

Karlsson, Susanne,Hallberg, Anders,Gronowitz, Salo

, p. 53 - 60 (2007/10/02)

The hydrozirconation of 9-(Z)-octadecenylmethyl-sulphide, 9-(Z)-octadecenyl phenyl sulphide and 9-(Z)-octadecenyl phenyl sulphone have been studied.These compounds underwent substantial elimination of the functional group, yielding after hydrolysis, along with saturated and unsaturated sulphides and sulphones, large amount of octadecane.The saturated analogues (dodecylmethyl-sulphide, octadecyl phenyl sulphide and octadecylphenyl sulphone) were unaffected by the hydrozirconation reagent under similar conditions.

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