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CAS

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67553-12-2

(R)-3-Methyl-5-oxo-5-phenyl-pentanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67553-12-2 Structure

  • Basic information

    1. Product Name: (R)-3-Methyl-5-oxo-5-phenyl-pentanoic acid
    2. Synonyms:
    3. CAS NO:67553-12-2
    4. Molecular Formula:
    5. Molecular Weight: 206.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67553-12-2.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: (R)-3-Methyl-5-oxo-5-phenyl-pentanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-3-Methyl-5-oxo-5-phenyl-pentanoic acid(67553-12-2)
    11. EPA Substance Registry System: (R)-3-Methyl-5-oxo-5-phenyl-pentanoic acid(67553-12-2)

  • 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: 67553-12-2(Hazardous Substances Data)

67553-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67553-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,5 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67553-12:
(7*6)+(6*7)+(5*5)+(4*5)+(3*3)+(2*1)+(1*2)=142
142 % 10 = 2
So 67553-12-2 is a valid CAS Registry Number.

67553-12-2Downstream Products

67553-12-2Relevant articles and documents

Asymmetric michael reactions : Enantioselective synthesis of δ-oxo-acids

Michelon, Francois,Pouilhes, Annie,Van Bac, Nguyen,Langlois, Nicole

, p. 1743 - 1746 (1992)

β-substituted and α,β-disubstituted δ-oxo acids are synthesized with high enantiomeric excess from chiral 2-propenyl oxazolines 8 and 11, whilst 2-vinyl oxazlines 7 and 10 are less efficient asymmetric inductors.

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