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CAS

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97510-06-0

Methyl 7-diphenylphosphinoyl-6-oxo-octanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97510-06-0 Structure

  • Basic information

    1. Product Name: Methyl 7-diphenylphosphinoyl-6-oxo-octanoate
    2. Synonyms: Methyl 7-diphenylphosphinoyl-6-oxo-octanoate
    3. CAS NO:97510-06-0
    4. Molecular Formula:
    5. Molecular Weight: 372.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97510-06-0.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: Methyl 7-diphenylphosphinoyl-6-oxo-octanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 7-diphenylphosphinoyl-6-oxo-octanoate(97510-06-0)
    11. EPA Substance Registry System: Methyl 7-diphenylphosphinoyl-6-oxo-octanoate(97510-06-0)

  • 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: 97510-06-0(Hazardous Substances Data)

97510-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97510-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97510-06:
(7*9)+(6*7)+(5*5)+(4*1)+(3*0)+(2*0)+(1*6)=140
140 % 10 = 0
So 97510-06-0 is a valid CAS Registry Number.

97510-06-0Relevant articles and documents

Synthesys of Single Isomers (E or Z) of Unsatured Carboxylic Acids by the Horner-Wittig Reaction

Levin, Daniel,Warren, Stuart

, p. 1799 - 1808 (2007/10/02)

Alkyl(diphenyl)phosphine oxides (5) are used to synthesize pure E or Z isomers of unsatured acids.The keto acids (10), made by two routes, are reduced to hydroxy acids whose crystalline lactones (12) can be separated and purified.Stereospecific elimination of Ph2PO2- gives the unsatured acids.

STEREOCHEMICALLY CONTROLLED SYNTHESIS OF UNSATURATED ACIDS VIA DIPHENYLPHOSPHINOYL(Ph2PO)-KETOACIDS

Levin, Daniel,Warren, Stuart

, p. 505 - 508 (2007/10/02)

Acylation of phosphine oxide anions with derivatives of cyclic anhydrides or oxidative cleavage of cyclic allyl phosphine oxides gives Ph2PO-ketoacids: reduction, separation of diastereoisomers, and completion of the Horner-Wittig reaction gives single isomers (E or Z) of unsaturated acids.

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