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13275-68-8

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13275-68-8 Usage

Chemical Properties

off-white needles

Safety Profile

Poison by intraperitoneal and subcutaneous routes. Experimental teratogenic effects. When heated to decomposition it emits very toxic fumes of NOx and SOx.

Check Digit Verification of cas no

The CAS Registry Mumber 13275-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13275-68:
(7*1)+(6*3)+(5*2)+(4*7)+(3*5)+(2*6)+(1*8)=98
98 % 10 = 8
So 13275-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H7N3S/c1-2-5-4-7-6-3-8-4/h3H,2H2,1H3,(H,5,7)

13275-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-1,3,4-thiadiazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-(3-PHENYL-5-ISOXAZOLYL)PHENOL

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:13275-68-8 SDS

13275-68-8Relevant articles and documents

Heterocyclization of thiocarbonohydrazides: Facile synthesis of 5-unsubstituted-1,3,4-thiadiazoles

Hassan, Alaa A.,Abdel-Latif, Fathy F.,Aziz, Mohamed Abdel,Mostafa, Sara M.,Br?se, Stefan,Nieger, Martin

, p. 1183 - 1186 (2015/09/01)

2-(Hydrazinecarbothioyl)-N-substituted hydrazinecarbothioamides react with 2,3,5,6-tetrachloro-1,4-benzoquinone in high yields in a novel fast and facile method to give 5-unsubstituted-1,3,4-thiadiazole-2-amine derivatives. The synthesized compounds were characterized by spectroscopic methods and confirmed by using X-ray crystallography. A rationale for the formation of the products is presented.

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