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(2S,3S)-2-azido-3-phenylisohexanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199468-81-0 Structure
  • Basic information

    1. Product Name: (2S,3S)-2-azido-3-phenylisohexanoic acid
    2. Synonyms: (2S,3S)-2-azido-3-phenylisohexanoic acid
    3. CAS NO:199468-81-0
    4. Molecular Formula:
    5. Molecular Weight: 233.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199468-81-0.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: (2S,3S)-2-azido-3-phenylisohexanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,3S)-2-azido-3-phenylisohexanoic acid(199468-81-0)
    11. EPA Substance Registry System: (2S,3S)-2-azido-3-phenylisohexanoic acid(199468-81-0)
  • 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: 199468-81-0(Hazardous Substances Data)

199468-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199468-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,4,6 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 199468-81:
(8*1)+(7*9)+(6*9)+(5*4)+(4*6)+(3*8)+(2*8)+(1*1)=210
210 % 10 = 0
So 199468-81-0 is a valid CAS Registry Number.

199468-81-0Downstream Products

199468-81-0Relevant articles and documents

Synthesis and conformational features of topographically constrained designer chimeric amino adds: The β-isopropyl phenylalanines

Liao, Subo,Shenderovich, Mark D.,Lin, Jun,Hruby, Victor J.

, p. 16645 - 16662 (2007/10/03)

All four optically pure isomers of the highly conformationally constrained novel chimeric amino acid, β-isopropylphenylalanine or β- phenylleucine, were asymmetrically synthesized in five to six steps in 20 - 25% overall yield. Computer-assisted molecular modeling revealed that the β- isopropyl group in these chimeric amino acids plays the dominant role in determining the most favorable side chain conformations.

Asymmetric synthesis of optically pure β-isopropylphenylalanine: A new β-branched unusual amino acid

Liao, Subo,Hruby, Victor J.

, p. 1563 - 1566 (2007/10/03)

All four optically pure isomers of a highly conformationally constrained unusual amino acid, β-isopropylphenylalanine, have been asymmetrically synthesized.

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