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Cyclopropanecarboxamide, 2-fluoro-2-phenyl-N-[(1S)-1-phenylethyl]-, (1S,2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

809282-77-7

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809282-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 809282-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,9,2,8 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 809282-77:
(8*8)+(7*0)+(6*9)+(5*2)+(4*8)+(3*2)+(2*7)+(1*7)=187
187 % 10 = 7
So 809282-77-7 is a valid CAS Registry Number.

809282-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S)-(-)-2-fluoro-2-phenylcyclopropyl-N-[(S)-1-phenylethyl]carboxamide

1.2 Other means of identification

Product number -
Other names (1S,2S)-2-Fluoro-2-phenyl-cyclopropanecarboxylic acid ((S)-1-phenyl-ethyl)-amide

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:809282-77-7 SDS

809282-77-7Upstream product

809282-77-7Relevant academic research and scientific papers

Fluorinated phenylcyclopropylamines. 2. Effects of aromatic ring substitution and of absolute configuration on inhibition of microbial tyramine oxidase

Rosen, Thomas C.,Yoshida, Shinichi,Fr?hlich, Roland,Kirk, Kenneth L.,Haufe, Günter

, p. 5860 - 5871 (2007/10/03)

A series of para-substituted diastereopure cis- and trans-2-fluoro-2- arylcyclopropylamines were synthesized and these were investigated as inhibitors of microbial tyramine oxidase from Arthrobacter sp. All compounds were shown to be competitive inhibitor

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