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151163-57-4

Methyl 6-(diethoxyphosphoryl)hexanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151163-57-4 Structure

  • Basic information

    1. Product Name: Methyl 6-(diethoxyphosphoryl)hexanoate
    2. Synonyms: Methyl 6-(diethoxyphosphoryl)hexanoate
    3. CAS NO:151163-57-4
    4. Molecular Formula: C11H23O7P
    5. Molecular Weight: 298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151163-57-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 6-(diethoxyphosphoryl)hexanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 6-(diethoxyphosphoryl)hexanoate(151163-57-4)
    11. EPA Substance Registry System: Methyl 6-(diethoxyphosphoryl)hexanoate(151163-57-4)

  • 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: 151163-57-4(Hazardous Substances Data)

151163-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151163-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,1,6 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 151163-57:
(8*1)+(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*5)+(1*7)=104
104 % 10 = 4
So 151163-57-4 is a valid CAS Registry Number.

151163-57-4Downstream Products

151163-57-4Relevant articles and documents

A comparison of phosphonothioic acids with phosphonic acids as phosphatase inhibitors

Swierczek, Krzysztof,Pandey, Arti S.,Peters, John W.,Hengge, Alvan C.

, p. 3703 - 3708 (2007/10/03)

Phosphorothioates, analogues of phosphate esters in which a sulfur replaces an oxygen atom in the phosphoryl group, are competent surrogate substrates for a number of phosphatases. In some cases the thio analogues show similar binding (as estimated by Ks

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