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50633-56-2

3β,6α-diacetoxy-22-tosyloxy-23,24-dinor-5α-cholane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 50633-56-2 Structure

  • Basic information

    1. Product Name: 3β,6α-diacetoxy-22-tosyloxy-23,24-dinor-5α-cholane
    2. Synonyms:
    3. CAS NO:50633-56-2
    4. Molecular Formula:
    5. Molecular Weight: 588.806
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 50633-56-2.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: 3β,6α-diacetoxy-22-tosyloxy-23,24-dinor-5α-cholane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3β,6α-diacetoxy-22-tosyloxy-23,24-dinor-5α-cholane(50633-56-2)
    11. EPA Substance Registry System: 3β,6α-diacetoxy-22-tosyloxy-23,24-dinor-5α-cholane(50633-56-2)

  • 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: 50633-56-2(Hazardous Substances Data)

50633-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50633-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50633-56:
(7*5)+(6*0)+(5*6)+(4*3)+(3*3)+(2*5)+(1*6)=102
102 % 10 = 2
So 50633-56-2 is a valid CAS Registry Number.

50633-56-2Downstream Products

50633-56-2Relevant articles and documents

Synthesis of 3β,6α-dihydroxy-5α-cholan-23-one

Nahar, Lutfun,Turner, Alan B.

, p. 8623 - 8628 (2003)

Evidence for the presence of 3β,6α-dihydroxy-5α -chol-9(11)-en-23-one in the aglycone mixture from the starfish Marthasterias glacialis is provided by the synthesis of 3β,6α-dihydroxy-5α -cholan-23-one (19) and its identification in the hydrogenated aglycone mixture. The side-chain is constructed from the 23,24-dinorcholanol (13) by reaction of the 22-tosylate (16) with the acetylide anion, followed by hydration of the resulting 23-yne (17).

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