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(2R,3R,4S,5R)-3-(benzyloxy)-5,7-dihydroxy-2,4-dimethylheptyl pivalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403660-75-2 Structure
  • Basic information

    1. Product Name: (2R,3R,4S,5R)-3-(benzyloxy)-5,7-dihydroxy-2,4-dimethylheptyl pivalate
    2. Synonyms: (2R,3R,4S,5R)-3-(benzyloxy)-5,7-dihydroxy-2,4-dimethylheptyl pivalate
    3. CAS NO:1403660-75-2
    4. Molecular Formula:
    5. Molecular Weight: 366.498
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403660-75-2.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: (2R,3R,4S,5R)-3-(benzyloxy)-5,7-dihydroxy-2,4-dimethylheptyl pivalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R,4S,5R)-3-(benzyloxy)-5,7-dihydroxy-2,4-dimethylheptyl pivalate(1403660-75-2)
    11. EPA Substance Registry System: (2R,3R,4S,5R)-3-(benzyloxy)-5,7-dihydroxy-2,4-dimethylheptyl pivalate(1403660-75-2)
  • 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: 1403660-75-2(Hazardous Substances Data)

1403660-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403660-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1403660-75:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*6)+(3*0)+(2*7)+(1*5)=132
132 % 10 = 2
So 1403660-75-2 is a valid CAS Registry Number.

1403660-75-2Relevant articles and documents

Total synthesis of (?)-tirandamycin c utilizing a desymmetrization protocol

Yadav,Dhara, Santu,Hossain, Sk. Samad,Mohapatra, Debendra K.

, p. 9628 - 9633 (2012)

A highly stereoselective total synthesis of (?)-tirandamycin C has been achieved following a desymmetrization protocol developed in our group, Horner-Wadsworth-Emmons olefination, acid-catalyzed ketalization, Still-Gennari (Z)-selective olefination, and D

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