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76689-65-1

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76689-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76689-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,8 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76689-65:
(7*7)+(6*6)+(5*6)+(4*8)+(3*9)+(2*6)+(1*5)=191
191 % 10 = 1
So 76689-65-1 is a valid CAS Registry Number.

76689-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-5-phenyl-3H-1,3,4-thiadiazole

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-5-phenyl-1,3,4-thiazoline-2

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:76689-65-1 SDS

76689-65-1Relevant articles and documents

Thiadiazoles and Dihydrothiadiazoles. Part 5. Synthesis of 2,3-Dihydro-1,3,4-thiadiazoles by Reaction of Aldehydes or Ketones with Thioaroylhydrazines

Evans, D. Michael,Hill, Lawrence,Taylor, David R.,Myers, Malcolm

, p. 1499 - 1506 (2007/10/02)

A general method for the synthesis of 2,5- and 2,2,5-substituted 2,3-dihydro-1,3,4-thiadiazoles is described, involving the condensation of aldehydes or ketones with thioaroylhydrazines.Evidence for the cyclic nature of the products is discussed.The react

SEMICARBAZONES AND THIOSEMICARBAZONES OF THE HETEROCYCLIC SERIES. XLIV. CYCLIZATION OF ISATIN AND 1-ACETYLISATIN 3-THIOBENZOYLHYDRAZONES

Tomchin, A.B.

, p. 504 - 510 (2007/10/02)

Isatin 3-thiobenzoylhydrazone undergoes cyclization with the addition of the sulfur atom to the C3 atom and closure of the thiadiazole ring.In contrast, 3-thioaroylhydrazones of 1-acetylisatin undergo cyclization with participation of C2 and close the thiadiazine ring with the formation of derivatives of the new heterocyclic system thiadiazinoindole.

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