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CAS

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126832-09-5

(4S,5R)-4-cyclohexylmethyl-2-oxazolidinone-5-carboxylic acid isopropyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126832-09-5 Structure

  • Basic information

    1. Product Name: (4S,5R)-4-cyclohexylmethyl-2-oxazolidinone-5-carboxylic acid isopropyl ester
    2. Synonyms: (4S,5R)-4-cyclohexylmethyl-2-oxazolidinone-5-carboxylic acid isopropyl ester
    3. CAS NO:126832-09-5
    4. Molecular Formula:
    5. Molecular Weight: 269.341
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126832-09-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4S,5R)-4-cyclohexylmethyl-2-oxazolidinone-5-carboxylic acid isopropyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5R)-4-cyclohexylmethyl-2-oxazolidinone-5-carboxylic acid isopropyl ester(126832-09-5)
    11. EPA Substance Registry System: (4S,5R)-4-cyclohexylmethyl-2-oxazolidinone-5-carboxylic acid isopropyl ester(126832-09-5)

  • 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: 126832-09-5(Hazardous Substances Data)

126832-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126832-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,3 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126832-09:
(8*1)+(7*2)+(6*6)+(5*8)+(4*3)+(3*2)+(2*0)+(1*9)=125
125 % 10 = 5
So 126832-09-5 is a valid CAS Registry Number.

126832-09-5Relevant articles and documents

Catalytic asymmetric direct α-amination reactions of 2-keto esters: A simple synthetic approach to optically active syn-β-amino-α-hydroxy esters

Juhl, Karsten,Jorgensen, Karl Anker

, p. 2420 - 2421 (2007/10/03)

The catalytic enantioselective direct α-amination reaction of 2-keto esters with easily available azo dicarboxylates as the nitrogen source and chiral bisoxazoline-copper(II) complexes as the catalyst is presented. The reations proceed with excellent enan

ORALLY ACTIVE RENIN INHIBITORS

-

, (2008/06/13)

This invention relates to compounds of the formula STR1 wherein Q, Z, D, E, R 3, R 4, R 5 and R 6 are defined as below, and the pharmaceutically acceptable salts thereof are disclosed. The compounds are useful as antihypertensive agents.

Orally active renin inhibitors

-

, (2008/06/13)

This invention relates to compounds of the formula wherein Q, Z, D, E, R3, R?, R? and R? are defined as below, and the pharmaceutically acceptable salts thereof are disclosed. The compounds are useful as antihypertensive agents.

Orally Potent Human Renin Inhibitors Derived from Angiotensinogen Transition State: Design, Synthesis, and Mode of Interaction

Iizuka, Kinji,Kamijo, Tetsuhide,Herada, Hiromu,Akahane, Kenji,Kubota, Tetsuhiro,et al.

, p. 2707 - 2714 (2007/10/02)

A three-dimensional structure of the complex of human renin and the scissile site P4 Pro to P1' Val of angiotensinogen was deduced in order to design potent human renin inhibitors rationally.On the basis of this structure, an orally

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