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893430-06-3

(R)-5-azido-7-(tert-butyldiphenylsilyloxy)heptanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 893430-06-3 Structure

  • Basic information

    1. Product Name: (R)-5-azido-7-(tert-butyldiphenylsilyloxy)heptanoic acid
    2. Synonyms: (R)-5-azido-7-(tert-butyldiphenylsilyloxy)heptanoic acid
    3. CAS NO:893430-06-3
    4. Molecular Formula:
    5. Molecular Weight: 425.603
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 893430-06-3.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: (R)-5-azido-7-(tert-butyldiphenylsilyloxy)heptanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-5-azido-7-(tert-butyldiphenylsilyloxy)heptanoic acid(893430-06-3)
    11. EPA Substance Registry System: (R)-5-azido-7-(tert-butyldiphenylsilyloxy)heptanoic acid(893430-06-3)

  • 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: 893430-06-3(Hazardous Substances Data)

893430-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 893430-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,4,3 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 893430-06:
(8*8)+(7*9)+(6*3)+(5*4)+(4*3)+(3*0)+(2*0)+(1*6)=183
183 % 10 = 3
So 893430-06-3 is a valid CAS Registry Number.

893430-06-3Relevant articles and documents

Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product

Yamauchi, Satoshi,Omi, Yasushi

, p. 1589 - 1594 (2008/02/02)

Optically pure (S)- and (R)-vinylpiperidine 2 and (S)-and (A)-(hydroxyethyl)piperidine 3, which were key intermediates for the synthesis of aloperine, were synthesized from yeast-reductive products.

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