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73501-03-8

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73501-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73501-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,0 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73501-03:
(7*7)+(6*3)+(5*5)+(4*0)+(3*1)+(2*0)+(1*3)=98
98 % 10 = 8
So 73501-03-8 is a valid CAS Registry Number.

73501-03-8SDS

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-bis(trichloromethyl)-5-(p-methoxyphenyl)-1,3,4-oxathiazole

1.2 Other means of identification

Product number -
Other names 5-(p-methoxyphenyl)-2,2-bis(trichloromethyl)-1,3,4-oxathiazole

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:73501-03-8 SDS

73501-03-8Relevant articles and documents

Nitrile Sulphides. Part 1. 1,3-Dipolar Cycloaddition to Carbonyl Groups activated by Trihaloalkyl Substituents; Synthesis and Crystal Structure of 1,3,4-Oxathiazoles

Damas, A. Margarida,Gould, Robert O.,Harding, Marjorie M.,Paton, R. Michael,Ross, John F.,Crosby, John

, p. 2991 - 2996 (2007/10/02)

Nitrile sulphides, generated by the thermal decarboxylation of 1,3,4-oxathiazol-2-ones, undergo 1,3-dipolar cycloaddition to the carbonyl group in chloral, hexachloroacetone and α,α,α-trifluoroacetophenone to yield 2,2,5-trisubstituted 1,3,4-oxathiazoles (18 - 76percent).Characterisation of the products is based on analytical and spectroscopic evidence, and is confirmed for 5-phenyl-2-trichloromethyl-1,3,4-oxathiazole and 5-(p-methoxyphenyl)-2-phenyl-2-trifluoromethyl-1,3,4-oxathiazole by X-ray crystal structure analyses.The oxathiazole rings are planar, with a localised C=N double bond.

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