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5ξ-Cholestan-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22033-82-5 Structure
  • Basic information

    1. Product Name: 5ξ-Cholestan-6-one
    2. Synonyms:
    3. CAS NO:22033-82-5
    4. Molecular Formula: C27H46O
    5. Molecular Weight: 386.65354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22033-82-5.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: 5ξ-Cholestan-6-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5ξ-Cholestan-6-one(22033-82-5)
    11. EPA Substance Registry System: 5ξ-Cholestan-6-one(22033-82-5)
  • 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: 22033-82-5(Hazardous Substances Data)

22033-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22033-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,3 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22033-82:
(7*2)+(6*2)+(5*0)+(4*3)+(3*3)+(2*8)+(1*2)=65
65 % 10 = 5
So 22033-82-5 is a valid CAS Registry Number.

22033-82-5Downstream Products

22033-82-5Relevant articles and documents

A Novel Method for Preparation of Steroidal Ketoximes from Nitroolefins

Habib, Rubina,Husain, Mubarak,Husain, Mashkoor,Khan, Naseem H.

, p. 801 (2007/10/02)

Steroidal 6-nitroolefins (I-IV) undergo facile reaction with NH3-MeOH-Zn yielding exclusively the corresponding 6-one oximes (V-VIII) in quantitative yields.The method appears to be of general applicability.

Reactions of epoxides-XXIV. The BF3-catalysed rearrangement of 4,5- and 5,6-epoxycholestanes

Blackett,Coxon,Hartshorn,Richards

, p. 4999 - 5005 (2007/10/07)

4α,5α, 4β,5β- and 5β, 6β-Epoxycholestanes give backbone rearranged compounds on BF3-catalysed rearrangement. Solvent changes markedly affect the products of rearrangement. 4α-Hydroxycompounds arise from the 4β,5β-epoxide on BF3-catal

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