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ethyl (2-thioxo-1,3-benzothiazol-3(2H)-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59794-33-1

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59794-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59794-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,9 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59794-33:
(7*5)+(6*9)+(5*7)+(4*9)+(3*4)+(2*3)+(1*3)=181
181 % 10 = 1
So 59794-33-1 is a valid CAS Registry Number.

59794-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-sulfanylidene-1,3-benzothiazol-3-yl)acetate

1.2 Other means of identification

Product number -
Other names (2-thioxo-benzothiazol-3-yl)-acetic acid ethyl ester

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:59794-33-1 SDS

59794-33-1Relevant academic research and scientific papers

A NEW ROUTE TO 2H-(1,2,4)TRIAZINO(3,4b)BENZOTHIAZOLE-3(4H)-ONE (4)

D'Amico, John J.,Bollinger, Frederic G.,Dahl, William E.

, p. 71 - 76 (2007/10/02)

The reaction of 3-(carbethoxymethyl)benzothiazoline-2-thione (1) with excess hydrazine in an aqueous medium at 25-30 deg or 95-100 deg C afforded the hydrazide (3) in 99percent yield and the titled heterocyclic compound (4) in 63percent yield, respectively.Under the same reaction conditions and replacing the above electrophile with 3-(carbethoxymethyl)-2-benzothiazoline furnished the hydrazide (5) in 45percent yield and a 6percent yield of 5 plus a high yield of a resinous mixture, respectively.Possible mechanism and supporting NMR and mass spectral data are discussed.

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