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(2R,3S,4R,5S) 5-azido-2,3,4-tris(benzyloxy) cycloheptane-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146236-96-6 Structure
  • Basic information

    1. Product Name: (2R,3S,4R,5S) 5-azido-2,3,4-tris(benzyloxy) cycloheptane-1-one
    2. Synonyms: (2R,3S,4R,5S) 5-azido-2,3,4-tris(benzyloxy) cycloheptane-1-one
    3. CAS NO:146236-96-6
    4. Molecular Formula:
    5. Molecular Weight: 471.556
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146236-96-6.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,3S,4R,5S) 5-azido-2,3,4-tris(benzyloxy) cycloheptane-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S,4R,5S) 5-azido-2,3,4-tris(benzyloxy) cycloheptane-1-one(146236-96-6)
    11. EPA Substance Registry System: (2R,3S,4R,5S) 5-azido-2,3,4-tris(benzyloxy) cycloheptane-1-one(146236-96-6)
  • 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: 146236-96-6(Hazardous Substances Data)

146236-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146236-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,3 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 146236-96:
(8*1)+(7*4)+(6*6)+(5*2)+(4*3)+(3*6)+(2*9)+(1*6)=136
136 % 10 = 6
So 146236-96-6 is a valid CAS Registry Number.

146236-96-6Downstream Products

146236-96-6Relevant articles and documents

Enantioselective syntheses of polyhydroxylated nortropane derivatives: Total synthesis of (+) and (-)-calystegine B2

Boyer, Francois-Didier,Lallemand, Jean-Yves

, p. 10443 - 10458 (2007/10/02)

(+) and (-)-Calystegine B2 were prepared from D-Glucose via Ferrier reaction followed by regiospecific ring enlargement of a polysubstituted cyclohexanone and intramolecular cyclisation of 4-aminocycloheptanone.

Polyhydroxylated nortropanes starting from D-glucose: Synthesis of homochiral (+) and ( -)-Calystegines B2

Duclos,Mondange,Dureault,Depezay

, p. 8061 - 8064 (2007/10/02)

The cycloheptano-isoxazoline 1, prepared from D-glucose, is converted to 6,7-dideoxy cycloheptitols which are suitable precursors for the synthesis of enantiomerically pure (+) and (-)-Calystegines B2.

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