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CAS

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131147-03-0

(+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131147-03-0 Structure

  • Basic information

    1. Product Name: (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol
    2. Synonyms: (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol
    3. CAS NO:131147-03-0
    4. Molecular Formula:
    5. Molecular Weight: 400.472
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131147-03-0.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: (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol(131147-03-0)
    11. EPA Substance Registry System: (+/-)-3,4-di-O-benzyl-1,2-O-isopropylidene-myo-inositol(131147-03-0)

  • 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: 131147-03-0(Hazardous Substances Data)

131147-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131147-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,4 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 131147-03:
(8*1)+(7*3)+(6*1)+(5*1)+(4*4)+(3*7)+(2*0)+(1*3)=80
80 % 10 = 0
So 131147-03-0 is a valid CAS Registry Number.

131147-03-0Relevant articles and documents

The synthesis and resolution of (+/-)-1,5,6-tri-O-benzyl-myo-inositol

Desai, Trupti,Fernandez-Mayoralas, Alfonso,Gigg, Jill,Gigg, Roy,Payne, Sheila

, p. 105 - 123 (2007/10/02)

Racemic 1,5,6-O-benzyl-myo-inositol was prepared by five routes and converted into 1,5,6-tri-O-benzyl-2,3-O-isopropylidene-myo-inositol, the camphanates of which were readily separated by chromatography.The absolute configurations of the chiral derivative

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