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13368-86-0

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13368-86-0 Usage

Chemical Properties

White crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 13368-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,6 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13368-86:
(7*1)+(6*3)+(5*3)+(4*6)+(3*8)+(2*8)+(1*6)=110
110 % 10 = 0
So 13368-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H2N2O2S/c6-3(7)2-1-4-8-5-2/h1H,(H,6,7)

13368-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5-THIADIAZOLE-3-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names thiadiazole carboxylic acid

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:13368-86-0 SDS

13368-86-0Relevant articles and documents

VINYL DERIVATIVES OF HETEROCYCLIC SYSTEMS AND THEIR POLIMERS: 3-VINYL-1,2,5-THIADIAZOLE

Bertini, V.,Lucchesini, F.,Munno, A. de

, p. 1245 - 1248 (1980)

3-Vinyl-1,2,5-thiadiazole is prepared by different methods: by one-pot reaction from 1,2,5-thiadiazole, by cyclization of 3,4-diamino-1-butene, and by the Wittig procedure either from 1,2,5-thiadiazolylmethylenetriphenylphosphorane or from 3-formyl-1,2,5-thiadiazole.Some physical and chemical properties are described.

4-[(4-(CARBOXYETHYL) PIPERIDINYL) METHYL] PYRROLIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

-

Page 32-33; 25, (2010/02/07)

3-Substituted pyrrolidines having a 4-carboxypiperidinylmethyl substituent on the 4-position of the ring are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.

Preparation of 1,2,5-Thiadiazole-3-carboxaldehydes

Mataka, Shuntaro,Kurisu, Masayoshi,Takahashi, Kazufumi,Tashiro, Masashi

, p. 325 - 328 (2007/10/02)

1,2,5-Thiadiazole-3-carboxaldehydes 1a-c were prepared by the acid-catalyzed decomposition of 3-azidomethyl-1,2,5-thiadiazoles 2a-c in 68-83percent yields, respectively.Pyrolysis of 2a and 2b afforded the imidazoles 4a and 4b in low yields.NBS-bromination of 1a and 1b gave the corresponding carboxylic acids 10a and 10b via acid bromides 9.Azides 2a and 2b gave the s-triazines 8a and 8b on treatment with NBS.

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