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17385-78-3

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17385-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17385-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17385-78:
(7*1)+(6*7)+(5*3)+(4*8)+(3*5)+(2*7)+(1*8)=133
133 % 10 = 3
So 17385-78-3 is a valid CAS Registry Number.

17385-78-3SDS

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 2-(4,5-dihydro-1,3-thiazol-2-ylsulfanyl)-1-phenylethanone

1.2 Other means of identification

Product number -
Other names 2-Phenacylmercaptothiazoline

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:17385-78-3 SDS

17385-78-3Relevant articles and documents

Formation of reagent-selective products from 2-(4,5-dihydrothi- azol-2-ylthio)-1-arylethanone with different nucleophiles

Saravanan,Mohan,Muthusubramanian

experimental part, p. 71 - 84 (2011/12/05)

The reactions of 2-(4,5-dihydrothiazol-2-ylthio)-1-arylethanone with different nucleophiles including semicarbazide hydrochloride, hydroxylamine hydrochloride, hydrazine, ethylenediamine and aminoethanol have been investigated, and the formation of a variety of products with different reagents is highlighted.

Studies on the Sructure of Some Derivatives of 1,3-Thiazolidine-2-thione and Δ2-1,3-Thiazoline-2-thiol

Fujita, Eiichi,Nagao, Yoshimitsu,Seno, Kaoru,Takao, Sachiko,Miyasaka, Tadayo,et al.

, p. 914 - 919 (2007/10/02)

Two types of reactions have been observed for the ambident anion of 1,3-thiazolidine-2-thione: regioselective N-acylation and S-alkylation.The structures of the products, amides and thioethers, were determined by X-ray crystallographic analysis and by ass

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