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883499-79-4

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883499-79-4 Usage

Type of compound

Chemical compound

Use as a reagent

Organic synthesis

Use as a protecting group

Chemical reactions

Derivative of

p-Toluenesulfonate

Known for

High stability and low reactivity

Industry use

Pharmaceutical industry (precursor for synthesis of organic compounds)

Additional uses

Surfactant, emulsifying agent, and other industrial applications

Versatility

Wide range of uses in chemical and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 883499-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,4,9 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 883499-79:
(8*8)+(7*8)+(6*3)+(5*4)+(4*9)+(3*9)+(2*7)+(1*9)=244
244 % 10 = 4
So 883499-79-4 is a valid CAS Registry Number.

883499-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4,5,5,5-nonafluoropentyl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 1H,1H-Perfluoropentyltosylate

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:883499-79-4 SDS

883499-79-4Downstream Products

883499-79-4Relevant articles and documents

Alternative synthetic routes to hydrofluoroolefins

Yagupolskii, Yu. L.,Pavlenko,Shelyazhenko,Filatov,Kremlev,Mushta,Gerus,Peng, Sheng,Petrov,Nappa, Mario

, p. 134 - 141 (2015/11/10)

A series of hydrofluoroolefins with -CF=CH2, -CH=CHF and -CH=CF2 groups were designed and prepared via various synthetic routes, including HX or BrF elimination, Wittig-type olefination or fluorination using SF4.

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