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313055-95-7

Cyclohexanecarboxamide, 2-amino-, (1S,2R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 313055-95-7 Structure

  • Basic information

    1. Product Name: Cyclohexanecarboxamide, 2-amino-, (1S,2R)- (9CI)
    2. Synonyms: Cyclohexanecarboxamide, 2-amino-, (1S,2R)- (9CI)
    3. CAS NO:313055-95-7
    4. Molecular Formula: C7H14N2O
    5. Molecular Weight: 142.19886
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 313055-95-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 321.8±31.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.073±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 16.65±0.40(Predicted)
    10. CAS DataBase Reference: Cyclohexanecarboxamide, 2-amino-, (1S,2R)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Cyclohexanecarboxamide, 2-amino-, (1S,2R)- (9CI)(313055-95-7)
    12. EPA Substance Registry System: Cyclohexanecarboxamide, 2-amino-, (1S,2R)- (9CI)(313055-95-7)

  • 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: 313055-95-7(Hazardous Substances Data)

313055-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 313055-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,0,5 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 313055-95:
(8*3)+(7*1)+(6*3)+(5*0)+(4*5)+(3*5)+(2*9)+(1*5)=107
107 % 10 = 7
So 313055-95-7 is a valid CAS Registry Number.

313055-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2R)-2-aminocyclohexanecarboxamide

1.2 Other means of identification

Product number -
Other names (1S,2R)-2-Amino-cyclohexanecarboxylic acid 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:313055-95-7 SDS

313055-95-7Downstream Products

313055-95-7Relevant articles and documents

Antiamyloid phenylsulfonamides: N-cycloalkylcarboxamides derivatives

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Page/Page column 8, (2010/02/11)

A series of N-cycloalkylcarboxamide derivatives of N-benzyl benzenesulfonamides of Formula I are described. The compounds inhibit β-amyloid peptide (β-AP) production and are useful in the treatment of Alzheimer's Disease and other conditions characterized

Structure-based design and synthesis of phosphinate isosteres of phosphotyrosine for incorporation in Grb2-SH2 domain inhibitors. Part 1

Furet, Pascal,Caravatti, Giorgio,Denholm, Alastair A.,Faessler, Alex,Fretz, Heinz,Garcia-Echeverria, Carlos,Gay, Brigitte,Irving, Ed,Press, Neil J.,Rahuel, Joseph,Schoepfer, Joseph,Walker, Clive V.

, p. 2337 - 2341 (2007/10/03)

Based on X-ray crystal structure information, mono charged phosphinate isosteres of phosphotyrosine have been designed and incorporated in a short inhibitory peptide sequence of the Grb2-SH2 domain. The resulting compounds, by exploiting additional interactions, inhibit binding to the Grb2-SH2 domain as potently as the corresponding doubly charged (phosphonomethyl)phenylalanine analogue. (C) 2000 Elsevier Science Ltd.

5,6-Dihydropyrimidin-4(3H)one derivatives, and antiedema compositions and methods employing them

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, (2008/06/13)

An antiedema compound of the formula: STR1 in which R1 is methyl, ethyl, cyclohexyl, phenyl, m-tolyl, p-tolyl, p-tert-butylphenyl, m-trifluoromethylphenyl, m-fluorophenyl, p-fluorophenyl, m-chlorophenyl, p-chlorophenyl, m-bromophenyl, p-bromoph

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