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β-chloro-β-phenylalanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 229485-67-0 Structure
  • Basic information

    1. Product Name: β-chloro-β-phenylalanine
    2. Synonyms: β-chloro-β-phenylalanine
    3. CAS NO:229485-67-0
    4. Molecular Formula:
    5. Molecular Weight: 199.637
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 229485-67-0.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: β-chloro-β-phenylalanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: β-chloro-β-phenylalanine(229485-67-0)
    11. EPA Substance Registry System: β-chloro-β-phenylalanine(229485-67-0)
  • 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: 229485-67-0(Hazardous Substances Data)

229485-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 229485-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,9,4,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 229485-67:
(8*2)+(7*2)+(6*9)+(5*4)+(4*8)+(3*5)+(2*6)+(1*7)=170
170 % 10 = 0
So 229485-67-0 is a valid CAS Registry Number.

229485-67-0Relevant articles and documents

ON THE SYNTHESIS OF β-PHENYLALANINE

Portelli, Mario

, p. 215 - 216 (2007/10/02)

A practical, economical and efficient two-step synthesis of β-phenylalanine and its methyl ester is reported: ?-phenylserine, 1, is chlorinated to β-chloro-β-phenylalanine, 2; the latter is hydrogenated in the presence of 10percent Pd/C catalyst to give the desired amino acid. β-Phenylalanine is separated (yield based upon β-phenylserine) as the free amino acid 3 (65.3percent yield) or as the hydrochloride 4 (79.8percent yield) or esterified to the methyl ester hydrochloride 5 (78.7percent yield).

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