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Benzeneacetic acid, a-aMino-2-hydroxy-, Methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 252967-15-0 Structure
  • Basic information

    1. Product Name: Benzeneacetic acid, a-aMino-2-hydroxy-, Methyl ester
    2. Synonyms: Benzeneacetic acid, a-aMino-2-hydroxy-, Methyl ester
    3. CAS NO:252967-15-0
    4. Molecular Formula: C9H11NO3
    5. Molecular Weight: 181.18854
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 252967-15-0.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: Benzeneacetic acid, a-aMino-2-hydroxy-, Methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzeneacetic acid, a-aMino-2-hydroxy-, Methyl ester(252967-15-0)
    11. EPA Substance Registry System: Benzeneacetic acid, a-aMino-2-hydroxy-, Methyl ester(252967-15-0)
  • 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: 252967-15-0(Hazardous Substances Data)

252967-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252967-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,9,6 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 252967-15:
(8*2)+(7*5)+(6*2)+(5*9)+(4*6)+(3*7)+(2*1)+(1*5)=160
160 % 10 = 0
So 252967-15-0 is a valid CAS Registry Number.

252967-15-0Downstream Products

252967-15-0Relevant articles and documents

Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine

Inada, Haruki,Shibuya, Masatoshi,Yamamoto, Yoshihiko

, p. 11047 - 11059 (2020/10/12)

The transamination of α-keto acids with 2-phenylglycine is an effective methodology for directly synthesizing unprotected α-amino acids. However, the synthesis of 2-arylglycines by transamination is problematic because the corresponding products, 2-arylglycines, transaminate the starting arylglyoxylic acids. Herein, we demonstrate the use of commercially available l-2-(2-chlorophenyl)glycine as the nitrogen source in the transamination of arylglyoxylic acids, producing the corresponding 2-arylglycines without interference from the undesired self-transamination process.

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