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CAS

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176589-78-9

1D-2-O-acetyl-1-O-butyryl-4,6-O-dibenzoyl-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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  • 176589-78-9 Structure

  • Basic information

    1. Product Name: 1D-2-O-acetyl-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol
    2. Synonyms: 1D-2-O-acetyl-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol
    3. CAS NO:176589-78-9
    4. Molecular Formula:
    5. Molecular Weight: 500.502
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176589-78-9.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: 1D-2-O-acetyl-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1D-2-O-acetyl-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol(176589-78-9)
    11. EPA Substance Registry System: 1D-2-O-acetyl-1-O-butyryl-4,6-O-dibenzoyl-myo-inositol(176589-78-9)

  • 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: 176589-78-9(Hazardous Substances Data)

176589-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176589-78-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,5,8 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 176589-78:
(8*1)+(7*7)+(6*6)+(5*5)+(4*8)+(3*9)+(2*7)+(1*8)=199
199 % 10 = 9
So 176589-78-9 is a valid CAS Registry Number.

176589-78-9Relevant articles and documents

Enzyme assisted synthesis of D-myo-inositol-1,2,6-trisphosphate

Andersch,Schneider

, p. 349 - 352 (1996)

The title compound is prepared in enantiomerically pure form via a facile enzyme assisted route. Essential for the success of the described method were a) the highly enantioselective esterification of 4,6-O-dibenzoyl-myo-inositol 2, b) the selective acylation of the axial hydroxyl function in 3 and c) the selective, base catalysed methanolysis of one benzoate group in 5. The obtained, selectively protected 1,2,6-triol 6 was converted into the title compound 7 by phosphorylation using N,N-dimethyl dibenzyl phosphoamidite followed by deprotection.

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