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CAS

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457614-07-2

(2S,5S,6S)-5-azido-6-benzyloxy-2-[(tert-butoxycarbonyl)amino]-1,8-[(methylsulfonyl)oxy]octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 457614-07-2 Structure

  • Basic information

    1. Product Name: (2S,5S,6S)-5-azido-6-benzyloxy-2-[(tert-butoxycarbonyl)amino]-1,8-[(methylsulfonyl)oxy]octane
    2. Synonyms: (2S,5S,6S)-5-azido-6-benzyloxy-2-[(tert-butoxycarbonyl)amino]-1,8-[(methylsulfonyl)oxy]octane
    3. CAS NO:457614-07-2
    4. Molecular Formula:
    5. Molecular Weight: 564.681
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 457614-07-2.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: (2S,5S,6S)-5-azido-6-benzyloxy-2-[(tert-butoxycarbonyl)amino]-1,8-[(methylsulfonyl)oxy]octane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,5S,6S)-5-azido-6-benzyloxy-2-[(tert-butoxycarbonyl)amino]-1,8-[(methylsulfonyl)oxy]octane(457614-07-2)
    11. EPA Substance Registry System: (2S,5S,6S)-5-azido-6-benzyloxy-2-[(tert-butoxycarbonyl)amino]-1,8-[(methylsulfonyl)oxy]octane(457614-07-2)

  • 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: 457614-07-2(Hazardous Substances Data)

457614-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 457614-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,7,6,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 457614-07:
(8*4)+(7*5)+(6*7)+(5*6)+(4*1)+(3*4)+(2*0)+(1*7)=162
162 % 10 = 2
So 457614-07-2 is a valid CAS Registry Number.

457614-07-2Relevant articles and documents

Enantioselective allyltitanation. Synthesis of (-)-slaframine

Cossy, Janine,Willis, Catherine,Bellosta, Ve?ronique,Saint-Jalmes, Laurent

, p. 951 - 957 (2007/10/03)

An enantioselective synthesis of the indolizidine alkaloid (-)-slaframine from aldehyde 1 is reported. The stereogenic centers at C-1 and C-8a are introduced by an enantioselective allyltitanation and a Mitsunobu reaction. Reductive double cyclization of

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