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CAS

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85483-00-7

3-Deoxyaphidicolin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85483-00-7 Structure

  • Basic information

    1. Product Name: 3-Deoxyaphidicolin
    2. Synonyms: 3-Deoxyaphidicolin
    3. CAS NO:85483-00-7
    4. Molecular Formula: C20H34O3
    5. Molecular Weight: 322.48216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85483-00-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 467.3°Cat760mmHg
    3. Flash Point: 210.2°C
    4. Appearance: /
    5. Density: 1.15g/cm3
    6. Vapor Pressure: 1.07E-10mmHg at 25°C
    7. Refractive Index: 1.568
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-Deoxyaphidicolin(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Deoxyaphidicolin(85483-00-7)
    12. EPA Substance Registry System: 3-Deoxyaphidicolin(85483-00-7)

  • 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: 85483-00-7(Hazardous Substances Data)

85483-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85483-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,8 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85483-00:
(7*8)+(6*5)+(5*4)+(4*8)+(3*3)+(2*0)+(1*0)=147
147 % 10 = 7
So 85483-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O3/c1-17(12-21)6-3-7-18(2)16(17)5-4-14-10-15-11-19(14,18)8-9-20(15,23)13-22/h14-16,21-23H,3-13H2,1-2H3/t14-,15+,16-,17-,18-,19?,20-/m0/s1

85483-00-7Downstream Products

85483-00-7Relevant articles and documents

Biosynthesis of diterpenoid aphidicolin: Isolation of intermediates from P-450 inhibitor treated mycelia of Phoma betae

Oikawa, Hideaki,Ohashi, Satoshi,Ichihara, Akitami,Sakamura, Sadao

, p. 7541 - 7554 (2007/10/03)

Treatment of Phoma betae with P-450 inhibitors caused accumulation of biosynthetic precursors 2, 3 and 4 of aphidicolin (1). Their structures were elucidated by spectroscopic analysis and they were confirmed by chemical transformations from 1. Isotopicall

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