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25814-82-8

5α-Androstan-12α-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25814-82-8 Structure

  • Basic information

    1. Product Name: 5α-Androstan-12α-ol
    2. Synonyms:
    3. CAS NO:25814-82-8
    4. Molecular Formula: C19H32O
    5. Molecular Weight: 276.45678
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25814-82-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5α-Androstan-12α-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5α-Androstan-12α-ol(25814-82-8)
    11. EPA Substance Registry System: 5α-Androstan-12α-ol(25814-82-8)

  • 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: 25814-82-8(Hazardous Substances Data)

25814-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25814-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,1 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25814-82:
(7*2)+(6*5)+(5*8)+(4*1)+(3*4)+(2*8)+(1*2)=118
118 % 10 = 8
So 25814-82-8 is a valid CAS Registry Number.

25814-82-8Downstream Products

25814-82-8Relevant articles and documents

COMPLEX HYDRIDE REDUCTIONS OF 12-OXOSTEROIDS. INFLUENCE OF REMOTE SUBSTITUENTS

Biesemans, M.,Woude, G. Van de,Hove, L. van

, p. 29 - 40 (2007/10/02)

A number of 12-oxosteroids with both 5α- and 5β-configuration and with variable side chain are reduced with LiAlH4, NaAlH4 and Li in THF and diethylether.The ratio of the epimeric 12-alcohols obtained, exhibits a remarkable dependence on the type of A/B ring fusion and on the C-17 substitution.An evaluation of these effects is made in the light of generally accepted rationalizations on the mechanism of ketone reductions by hydride reagents.

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