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CAS

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582295-24-7

(2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 582295-24-7 Structure

  • Basic information

    1. Product Name: (2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester
    2. Synonyms: (2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester
    3. CAS NO:582295-24-7
    4. Molecular Formula:
    5. Molecular Weight: 254.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 582295-24-7.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: (2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester(582295-24-7)
    11. EPA Substance Registry System: (2S,3R)-2-amino-3-hydroxy-3-(4-nitro-phenyl)-propionic acid ethyl ester(582295-24-7)

  • 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: 582295-24-7(Hazardous Substances Data)

582295-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 582295-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,2,9 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 582295-24:
(8*5)+(7*8)+(6*2)+(5*2)+(4*9)+(3*5)+(2*2)+(1*4)=177
177 % 10 = 7
So 582295-24-7 is a valid CAS Registry Number.

582295-24-7Relevant articles and documents

An enantioselective synthesis of nitrogen protected 3-arylserine esters

Bourdon, Lisa H.,Fairfax, David J.,Martin, Gregory S.,Mathison, Casey J.,Zhichkin, Pavel

, p. 3485 - 3487 (2007/10/03)

A method for the preparation of (2R,3S) nitrogen protected arylserine esters is described. The method consists of rhodium mediated insertion of tert-butylcarbamate into the corresponding 3-keto-2-diazoester, affording the N-protected α-amino-β-ketoester, followed by asymmetric reduction/dynamic resolution to afford the corresponding N-protected 3-arylserine esters in good chemical yield, and in most cases high enantiomeric excess.

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