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58274-46-7

(22E)-3α,5-cyclo-6β-hydroxy-5α-stigmast-22-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58274-46-7 Structure

  • Basic information

    1. Product Name: (22E)-3α,5-cyclo-6β-hydroxy-5α-stigmast-22-ene
    2. Synonyms: (22E)-3α,5-cyclo-6β-hydroxy-5α-stigmast-22-ene
    3. CAS NO:58274-46-7
    4. Molecular Formula:
    5. Molecular Weight: 412.7
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58274-46-7.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: (22E)-3α,5-cyclo-6β-hydroxy-5α-stigmast-22-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (22E)-3α,5-cyclo-6β-hydroxy-5α-stigmast-22-ene(58274-46-7)
    11. EPA Substance Registry System: (22E)-3α,5-cyclo-6β-hydroxy-5α-stigmast-22-ene(58274-46-7)

  • 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: 58274-46-7(Hazardous Substances Data)

58274-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58274-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,7 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58274-46:
(7*5)+(6*8)+(5*2)+(4*7)+(3*4)+(2*4)+(1*6)=147
147 % 10 = 7
So 58274-46-7 is a valid CAS Registry Number.

58274-46-7Relevant articles and documents

Solvolysis of sterol tosylates in aqueous dimethylformamide

Kovganko,Survilo

, p. 324 - 327 (1999)

It has been established that the heating of the sterol tosylates (1a - c) in aqueous dimethylformamide in the presence of sodium acetate leads to the formation of the 3α,5-cyclo-6β-alcohols (2), the sterols (3), the 3,5-dienes (4), and the sterol formates (5).

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