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CAS

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1010104-76-3

(3aR,7aR)-3-(4-benzyloxybenzoyl)-4,5-dihydroxyhexahydrobenzoxazol-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1010104-76-3 Structure

  • Basic information

    1. Product Name: (3aR,7aR)-3-(4-benzyloxybenzoyl)-4,5-dihydroxyhexahydrobenzoxazol-2-one
    2. Synonyms: (3aR,7aR)-3-(4-benzyloxybenzoyl)-4,5-dihydroxyhexahydrobenzoxazol-2-one
    3. CAS NO:1010104-76-3
    4. Molecular Formula:
    5. Molecular Weight: 383.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1010104-76-3.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: (3aR,7aR)-3-(4-benzyloxybenzoyl)-4,5-dihydroxyhexahydrobenzoxazol-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3aR,7aR)-3-(4-benzyloxybenzoyl)-4,5-dihydroxyhexahydrobenzoxazol-2-one(1010104-76-3)
    11. EPA Substance Registry System: (3aR,7aR)-3-(4-benzyloxybenzoyl)-4,5-dihydroxyhexahydrobenzoxazol-2-one(1010104-76-3)

  • 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: 1010104-76-3(Hazardous Substances Data)

1010104-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1010104-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,1,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1010104-76:
(9*1)+(8*0)+(7*1)+(6*0)+(5*1)+(4*0)+(3*4)+(2*7)+(1*6)=53
53 % 10 = 3
So 1010104-76-3 is a valid CAS Registry Number.

1010104-76-3Downstream Products

1010104-76-3Relevant articles and documents

Chiral version of the burgess reagent and its reactions with oxiranes: Application to the formal enantiodivergent synthesis of balanol

Sullivan, Bradford,Gilmet, Jacqueline,Leisch, Hannes,Hudlicky, Tomas

, p. 346 - 350 (2008)

An efficient formal synthesis of a (-)-balanol intermediate (25a) from cyclohexadiene oxide was accomplished in eight steps. An asymmetric version of the Burgess reagent allows for an enantiodivergent approach to both enantiomers of balanol from a racemic starting material.

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