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179337-57-6

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179337-57-6 Usage

Uses

1-(4,5-Dihydro-2-thiazolyl)-3-azetidinethiol Hydrochloride is used as a reagent in the synthesis of Tebipenem Tetrahydrate (T012840); the active metabolite of Tebipenem Pivoxil (T012900) that shows excellent bactericidal activity against β-lactamase-nonproducing, ampicillin-resistant isolates.

Check Digit Verification of cas no

The CAS Registry Mumber 179337-57-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,3,3 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 179337-57:
(8*1)+(7*7)+(6*9)+(5*3)+(4*3)+(3*7)+(2*5)+(1*7)=176
176 % 10 = 6
So 179337-57-6 is a valid CAS Registry Number.

179337-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4,5-dihydro-1,3-thiazol-2-yl)azetidine-3-thiol,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(4,5-Dihydro-2-thiazolyl)-3-azetidinethiol HCl

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:179337-57-6 SDS

179337-57-6Downstream Products

179337-57-6Relevant articles and documents

An efficient method for the synthesis of 3-mercapto-1-(1,3-thiazolin-2-YL)Azetidine useful for the pendant moiety of oral carbapenem, L-084

Isoda, Takeshi,Tamai, Satoshi,Kumagai, Toshio,Nagao, Yoshimitsu

, p. 1821 - 1824 (2006)

An efficient method for the synthesis of 3-mercapto-1-(1,3-thiazolin-2-yl)azetidine (1) is described. This thiol synthesis was achieved in 3 steps from readily available 3-methanesulfonyloxyazetidine via key intermediates, Bunte salts (3 and 5). The final step was enabled to proceed under mild conditions using the benzylthiol-mediated cleavage of the S-S bond in the Bunte salt (3).{A figure is presented}.

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