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2-Benzothiazolamine,6-chloro-N-ethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84016-92-2

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84016-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84016-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84016-92:
(7*8)+(6*4)+(5*0)+(4*1)+(3*6)+(2*9)+(1*2)=122
122 % 10 = 2
So 84016-92-2 is a valid CAS Registry Number.

84016-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl-(6-chloro-benzothiazol-2-yl)-amine

1.2 Other means of identification

Product number -
Other names (6-Chloro-benzothiazol-2-yl)-ethyl-amine

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:84016-92-2 SDS

84016-92-2Downstream Products

84016-92-2Relevant academic research and scientific papers

Microwave assisted one pot synthesis of 2-ethylamino benzimidazole, benzoxazole and benzothiazole derivatives

Rapolu, Thirupathi,K. V. P, Pavan Kumar,Babu, Korupolu Raghu,Dende, Satheesh Kumar,Nimmareddy, Rajashekar Reddy,Reddy, Leleti Krishnakanth

supporting information, p. 1308 - 1315 (2019/04/30)

A rapid and efficient one-pot method for the synthesis of 2-ethylamino benzimidazole, benzoxazole, and benzothiazole derivatives has been described. The reaction of o-phenylenediamines or o-aminophenols or 2-mercaptoanilines with EDC.HCl under microwave irradiation afforded the corresponding 2-ethylamino benzimidazole, benzoxazole and benzothiazole derivatives in excellent yields.

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