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89569-19-7

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89569-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89569-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,6 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89569-19:
(7*8)+(6*9)+(5*5)+(4*6)+(3*9)+(2*1)+(1*9)=197
197 % 10 = 7
So 89569-19-7 is a valid CAS Registry Number.

89569-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-2-ethyl-4H-1,4-benzothiazin-3-one

1.2 Other means of identification

Product number -
Other names -

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:89569-19-7 SDS

89569-19-7Downstream Products

89569-19-7Relevant articles and documents

Synergistic promoting effect of ball milling and KF-alumina support for the green synthesis of benzothiazinones

Sharifi, Ali,Ansari, Mohammad,Darabi, Hossein Reza,Abaee, M. Saeed

, p. 529 - 532 (2016)

A solvent-free procedure was developed for the reaction of 2-aminothiophenols with 2-bromoalkanoates, where KF-Al2O3 support and ball milling cooperatively lead to a green and efficient synthesis of several benzothiazinone derivatives in good to excellent yields. The catalyst could be recycled in further reactions while maintaining its activity.

Regioselective one pot synthesis of 2-alkyl/aryl-4H-benzo[1,4]thiazine-3- one via microwave irradiation

Kamila, Sukanta,Koh, Benjamin,Khan, Omair,Zhang, Hongming,Biehl, Edward R.

, p. 1641 - 1646 (2007/10/03)

A series of 2-alkyl/aryl-4H-benzo[1,4]thiazine-3-ones have been synthesized by microwave irradiation of ethyl-2-bromo-2-alkyl/aryl acetate and 2-amino thiophenol in the presence of 1,8-diazabicyclo-[5.4.0]undec-7-ene and N-methylpiperidine. All compounds were characterized by 1H NMR, 13C NMR and elemental analyses, and by X-ray crystallography in the case of 2-methyl-4H-benzo[1,4]thiazin-3-one.

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