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10561-30-5

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10561-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10561-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10561-30:
(7*1)+(6*0)+(5*5)+(4*6)+(3*1)+(2*3)+(1*0)=65
65 % 10 = 5
So 10561-30-5 is a valid CAS Registry Number.

10561-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(1,3-benzothiazol-2-yl) ethanethioate

1.2 Other means of identification

Product number -
Other names 1-benzothiazol-2-ylthioethan-1-one

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:10561-30-5 SDS

10561-30-5Relevant articles and documents

Fly-ash-supported synthesis of 2-mercaptobenzothiazole derivatives under microwave irradiation

Narkhede, Hemant P.,More, Uttam B.,Dalal, Dipak S.,Pawar, Nilesh S.,More, Dhananjay H.,Mahulikar, Pramod P.

, p. 575 - 579 (2007/10/03)

Microwave-assisted, solvent-free alkylation and acylation of 2-mercaptobenzothiazole has been attempted using silica gel, alumina, and a new solid support, fly ash. Fly ash, a waste generated at thermal power stations, could be used as solid support just as efficiently as commercial supports. The additional features of methodology include a much faster reaction, easy workup, higher yields, higher purity of the products, and an ecofriendly approach. Copyright Taylor & Francis Group, LLC.

Acylation and alkoxycarbonylation of benzoxazoline-2-thione and benzothiazoline-2-thione

Nishio, Takehiko,Shiwa, Kiyoko

, p. 313 - 324 (2007/10/03)

Acylation of benzoxazoline-2-thione (1) and benzothiazoline-2-thione (2) with acetic anhydride (3) and acyl chlorides (4) gave N-acyl (5, 6) and/or S-acyl (7, 8) derivatives depending on the nature of acylating agents and bases used. Alkoxycarbonylation of 1 with aralkyl chlorocarbonates (9) gave N-alkoxycarbonyl derivatives (10) mainly, while that of 2 with aralkyl chloroccarbonates (9) gave S-alkoxycarbonyl derivatives (12) exclusively. Photolysis of N-acyl derivatives (5 or 6) in the presence of alcohols afforded 1 or 2, respectively, together with esters (16).

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