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CAS

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844867-09-0

L-Phenylalanine, a-methyl-N,N-bis(phenylmethyl)-, 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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  • 844867-09-0 Structure

  • Basic information

    1. Product Name: L-Phenylalanine, a-methyl-N,N-bis(phenylmethyl)-, methyl ester
    2. Synonyms:
    3. CAS NO:844867-09-0
    4. Molecular Formula: C25H27NO2
    5. Molecular Weight: 373.495
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 844867-09-0.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: L-Phenylalanine, a-methyl-N,N-bis(phenylmethyl)-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Phenylalanine, a-methyl-N,N-bis(phenylmethyl)-, methyl ester(844867-09-0)
    11. EPA Substance Registry System: L-Phenylalanine, a-methyl-N,N-bis(phenylmethyl)-, methyl ester(844867-09-0)

  • 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: 844867-09-0(Hazardous Substances Data)

844867-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844867-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,8,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 844867-09:
(8*8)+(7*4)+(6*4)+(5*8)+(4*6)+(3*7)+(2*0)+(1*9)=210
210 % 10 = 0
So 844867-09-0 is a valid CAS Registry Number.

844867-09-0Relevant articles and documents

Enantiocontrolled synthesis of α-methyl amino acids via Bn 2N-α-methylserine-β-lactone

Smith, Nicole D.,Wohlrab, Aaron M.,Goodman, Murray

, p. 255 - 258 (2007/10/03)

(Chemical Equation Presented) Enantiocontrolled synthesis of α-methyl amino acids proceeds via the regioselective organocuprate opening of Bn 2N-α-methylserine-β-lactone. From this chiral intermediate, a wide variety of α-methyl amino acids and

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