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63140-93-2

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63140-93-2 Usage

Structure

Cyclopropane derivative with an amino group and a phenyl group attached to the cyclopropane ring

Pharmaceutical applications

Acts as a ligand for various receptors and enzymes

Biological activity

Modulator of the GABA receptor

Potential use

Treatment of anxiety and other central nervous system disorders

Research focus

Building block for the synthesis of novel chemical compounds with potential medicinal properties

Check Digit Verification of cas no

The CAS Registry Mumber 63140-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,4 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63140-93:
(7*6)+(6*3)+(5*1)+(4*4)+(3*0)+(2*9)+(1*3)=102
102 % 10 = 2
So 63140-93-2 is a valid CAS Registry Number.

63140-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-2-phenyl-1-aminocyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-AMINO-2-PHENYLCYCLOPROPANECARBOXYLIC ACID

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:63140-93-2 SDS

63140-93-2Relevant articles and documents

USP30 INHIBITORS AND USES THEREOF

-

Paragraph 00491-00492, (2021/03/19)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of USP30, and the treatment of USP30-mediated disorders.

1-Aminocyclopropane-1-carboxylic acid derivatives: A new, general synthesis and NMDA receptor complex binding affinity study

Spadoni,Balsamini,Bedini,Mugnaini

, p. 1663 - 1674 (2007/10/02)

A new synthesis of 1-aminocyclopropane-1-carboxylic acid and of its (E)- and (Z)-2-substituted analogues (R = CH3;i-Pr;C6H5) has been performed by means of the 'diazo-addition' method, starting from N-(diphenylmethylene)-2,3-dehydro-1-amino-1-carboxylate precursors. The (E)- and (Z)-2-phenyl and the (Z)-2-methylcyclopropaneamino acids have been obtained with high diastereospecificity. All the cyclopropaneamino acids prepared were tested for their affinity for some glutamate receptors and resulted inactive, wich the exception of compounds (E)-1b and (Z)-1c which showed a shallow displacement of [H]-glycine binding.

SYNTHESIS OF 1-AZIDOCYCLOPROPANECARBOXYLATES FROM 2-AZIDO-2-ALKENOATES

Hiyama, Tamejiro,Kai, Mariko

, p. 2103 - 2104 (2007/10/02)

Addition of diazomethane to 2-azido-2-alkenoates followed by pyrolysis of the resulting pyrazoline derivatives affords the title compounds.

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