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CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124753-65-7 Structure
  • Basic information

    1. Product Name: CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID
    2. Synonyms: CIS-1-(BENZYLOXYCARBONYL-AMINO)-CYCLOHEX-4-ENYL-2-CARBOXYLIC ACID;CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID;CIS-6-BENZYLOXYCARBONYLAMINOCYCLOHEX-3-ENECARBOXYLIC ACID;Z-CIS-2-AMINOCYCLOHEXENECARBOXYLIC ACID;Z-1,2-CIS-ACHEC-OH;3-Cyclohexene-1-carboxylicacid,6-[[(phenylmethoxy)carbonyl]amino]-,(1R,6S)-rel-(9CI);cis-2-(Benzyloxycarbonylamino)-4-cyclohexene-1-carboxylic acid,98%;cis-6-(BenzyloxycarbonylaMino)-3-cyclohexene-1-carboxylic acid, 97%
    3. CAS NO:124753-65-7
    4. Molecular Formula: C15H17NO4
    5. Molecular Weight: 275.3
    6. EINECS: N/A
    7. Product Categories: N-CBZ
    8. Mol File: 124753-65-7.mol
  • Chemical Properties

    1. Melting Point: 118-124 °C
    2. Boiling Point: 418.25°C (rough estimate)
    3. Flash Point: 249.4°C
    4. Appearance: /Solid
    5. Density: 1.1552 (rough estimate)
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.5200 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID(124753-65-7)
    12. EPA Substance Registry System: CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID(124753-65-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 24/25
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124753-65-7(Hazardous Substances Data)

124753-65-7 Usage

Chemical Properties

off-white to beige powder

Check Digit Verification of cas no

The CAS Registry Mumber 124753-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,7,5 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124753-65:
(8*1)+(7*2)+(6*4)+(5*7)+(4*5)+(3*3)+(2*6)+(1*5)=127
127 % 10 = 7
So 124753-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO4/c17-14(18)12-8-4-5-9-13(12)16-15(19)20-10-11-6-2-1-3-7-11/h1-7,12-13H,8-10H2,(H,16,19)(H,17,18)/p-1/t12-,13+/m1/s1

124753-65-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H62650)  cis-6-(Benzyloxycarbonylamino)-3-cyclohexene-1-carboxylic acid, 97%   

  • 124753-65-7

  • 250mg

  • 840.0CNY

  • Detail
  • Alfa Aesar

  • (H62650)  cis-6-(Benzyloxycarbonylamino)-3-cyclohexene-1-carboxylic acid, 97%   

  • 124753-65-7

  • 1g

  • 2520.0CNY

  • Detail

124753-65-7SDS

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 CIS-2-(BENZYLOXYCARBONYLAMINO)-4-CYCLOHEXENE-1-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names Z-1,2-CIS-ACHEC-OH

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:124753-65-7 SDS

124753-65-7Relevant articles and documents

Stereoselective synthesis of hydroxylated β-aminocyclohexanecarboxylic acids

Kiss, Loránd,Forró, Eniko,Martinek, Tamás A.,Bernáth, Gábor,De Kimpe, Norbert,Fül?p, Ferenc

, p. 5036 - 5043 (2008/09/21)

A simple synthetic approach has been developed for the regio- and diastereoselective synthesis of hydroxylated 2-aminocyclohexanecarboxylic acid stereoisomers from 1,4-cyclohexadiene by the reductive opening of appropriate epoxide intermediates derived from the corresponding bicyclic β-lactams. This method has been extended to the synthesis of these hydroxylated β-amino acids in enantiomerically pure form.

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