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58324-02-0

3β,7α-dihydroxy-17a-aza-D-homoandrost-5-en-17-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58324-02-0 Structure

  • Basic information

    1. Product Name: 3β,7α-dihydroxy-17a-aza-D-homoandrost-5-en-17-one
    2. Synonyms:
    3. CAS NO:58324-02-0
    4. Molecular Formula:
    5. Molecular Weight: 319.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58324-02-0.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,7α-dihydroxy-17a-aza-D-homoandrost-5-en-17-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3β,7α-dihydroxy-17a-aza-D-homoandrost-5-en-17-one(58324-02-0)
    11. EPA Substance Registry System: 3β,7α-dihydroxy-17a-aza-D-homoandrost-5-en-17-one(58324-02-0)

  • 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: 58324-02-0(Hazardous Substances Data)

58324-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58324-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,2 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58324-02:
(7*5)+(6*8)+(5*3)+(4*2)+(3*4)+(2*0)+(1*2)=120
120 % 10 = 0
So 58324-02-0 is a valid CAS Registry Number.

58324-02-0Downstream Products

58324-02-0Relevant articles and documents

Microbiological Transformations. Part 5. Microbiological Transformations of 17a-Aza- and 17-Aza-D-homoandrost-5-ene Derivatives with the Fungus Cunninghamella elegans

Crabb, Trevor A.,Dawson, Philip J.,Williams, Roger O.

, p. 571 - 576 (2007/10/02)

The products obtained from the incubation of 17a-aza- and 17-aza-D-homoandrost-5-ene derivatives with Cunninghamella elegans are largely those resulting from allylic oxidation or epoxidation of the Δ5-bond.The substrates are predominantly monohydroxylated whereas androst-5-ene derivatives under the same conditions show a tendency towards dihydroxylation.

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