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Methanone, [2-[[2-(acetyloxy)ethyl]amino]-5-chlorophenyl](2-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60776-33-2

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60776-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60776-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60776-33:
(7*6)+(6*0)+(5*7)+(4*7)+(3*6)+(2*3)+(1*3)=132
132 % 10 = 2
So 60776-33-2 is a valid CAS Registry Number.

60776-33-2SDS

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 2-(2-Acetoxyethylamino)-5-chloro-2'-fluorobenzophenone

1.2 Other means of identification

Product number -
Other names Acetic acid 2-[4-chloro-2-(2-fluoro-benzoyl)-phenylamino]-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:60776-33-2 SDS

60776-33-2Upstream product

60776-33-2Downstream Products

60776-33-2Relevant academic research and scientific papers

Intermediates for tricyclic benzodiazepines

-

, (2008/06/13)

Tricyclic benzodiazepine derivatives ("A") bearing a hydroxylower alkyl substituent in the 1-position and a heterocyclic ring joined between positions 4 and 5 of the benzodiazepine moiety are described. The heterocyclic ring will contain the nitrogen atom appearing at position 4 of the benzodiazepine ring as well as the hetero atom, which may be either oxygen or nitrogen, attached to the carbon atom at the 5-position of the benzodiazepine ring. "A" bearing an oxygen atom in the new heterocyclic ring may be formed from the corresponding 4,5-unsaturated benzodiazepines by treatment with an epoxide compound in the presence of an acid catalyst. "A" bearing either a nitrogen or an oxygen atom in the new heterocyclic ring may be prepared by cyclization of the corresponding open compound. "A" are useful as sedative, muscle relaxant and anti-convulsant agents.

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