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CAS

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635318-20-6

Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-fluoro-, (1R,2S,4R,5R,6R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 635318-20-6 Structure

  • Basic information

    1. Product Name: Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-fluoro-, (1R,2S,4R,5R,6R)- (9CI)
    2. Synonyms: Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-fluoro-, (1R,2S,4R,5R,6R)- (9CI)
    3. CAS NO:635318-20-6
    4. Molecular Formula: C8H10FNO4
    5. Molecular Weight: 203.1677032
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 635318-20-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-fluoro-, (1R,2S,4R,5R,6R)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-fluoro-, (1R,2S,4R,5R,6R)- (9CI)(635318-20-6)
    11. EPA Substance Registry System: Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-fluoro-, (1R,2S,4R,5R,6R)- (9CI)(635318-20-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 635318-20-6(Hazardous Substances Data)

635318-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 635318-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,3,1 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 635318-20:
(8*6)+(7*3)+(6*5)+(5*3)+(4*1)+(3*8)+(2*2)+(1*0)=146
146 % 10 = 6
So 635318-20-6 is a valid CAS Registry Number.

635318-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S,4R,5R,6R)-2-amino-4-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2α-amino-4α-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic 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:635318-20-6 SDS

635318-20-6Downstream Products

635318-20-6Relevant articles and documents

Synthesis and pharmacological characterization of 4-substituted-2- aminobicyclo[3.1.0]hexane-2,6-dicarboxylates: Identification of new potent and selective metabotropic glutamate 2/3 receptor agonists

Monn, James A.,Valli, Matthew J.,Massey, Steven M.,Hao, Junliang,Reinhard, Matthew R.,Bures, Mark G.,Heinz, Beverly A.,Wang, Xushan,Carter, Joan H.,Getman, Brian G.,Stephenson, Gregory A.,Herin, Marc,Catlow, John T.,Swanson, Steven,Johnson, Bryan G.,McKinzie, David L.,Henry, Steven S.

, p. 4442 - 4455 (2013/07/19)

As part of our ongoing interest in identifying novel agonists acting at metabotropic glutamate (mGlu) 2/3 receptors, we have explored the effect of structural modifications of 1S,2S,5R,6S-2-aminobicyclo[3.1.0]hexane-2,6- dicarboxylate (LY354740), a potent

A method for the synthesis of 2-amino-4-fluorobicyclo[3.1.0]hexane-2,6- dicarboxylic acid-[3H2]

Kuo, Fengjiun,Kulanthaivel, Palaniappan,Rener, Gregory A.,Yi, Ping,Wheeler, William J.

, p. 571 - 581 (2007/10/03)

A process for double deuterium labeling of an alcohol was developed. The process was utilized in the subsequent tritium labeling of a secondary alcohol with high specific activity (24 Ci/mmol) by reduction of the corresponding ketone using sodium borotrit

PRODRUGS OF EXCITATORY AMINO ACIDS

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Page 110, (2008/06/13)

This invention relates to synthetic excitatory amino acid prodrugs and processes for their preparation. The invention further relates to methods of using, and pharmaceutical compositions comprising, the compounds for the treatment of neurological disorder

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