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38037-44-4

3β-Hydroxy-5,6β-cyclopropano-5β-cholestane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38037-44-4 Structure

  • Basic information

    1. Product Name: 3β-Hydroxy-5,6β-cyclopropano-5β-cholestane
    2. Synonyms: (5β)-3',6α-Dihydrocyclopropa[5,6]cholestan-3β-ol
    3. CAS NO:38037-44-4
    4. Molecular Formula: C28H48O
    5. Molecular Weight: 400.68012
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38037-44-4.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: 3β-Hydroxy-5,6β-cyclopropano-5β-cholestane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3β-Hydroxy-5,6β-cyclopropano-5β-cholestane(38037-44-4)
    11. EPA Substance Registry System: 3β-Hydroxy-5,6β-cyclopropano-5β-cholestane(38037-44-4)

  • 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: 38037-44-4(Hazardous Substances Data)

38037-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38037-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,3 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38037-44:
(7*3)+(6*8)+(5*0)+(4*3)+(3*7)+(2*4)+(1*4)=114
114 % 10 = 4
So 38037-44-4 is a valid CAS Registry Number.

38037-44-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-hydroxy-5,6β-cyclopropano-5β-cholestane

1.2 Other means of identification

Product number -
Other names 3β-Hydroxy-5,7α-cyclo-B-homo-5α-cholestan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38037-44-4 SDS

38037-44-4Relevant articles and documents

Microbial transformation of 3-hydroxy-5,6-cyclopropanocholestanes - An alternative route to 6-methylsteroids

Yan, Jiann-Long,Lee, Shoei-Sheng,Wang

, p. 863 - 870 (2007/10/03)

Incubation of 3β-hydroxy-5,6α-cyclopropano-5α-cholestane (4), 3β-hydroxy-5,6β-cyclopropano-5β-cholestane (5), and 3β-hydroxy-5,6α-cyclopropano-5α-cholest-7-ene (6) with Mycobacterium sp. (NRRL B-3805) gave a mixture of side chain cleaved 17-keto steroids as the major products in 52, 57, and 69% yields, respectively. Among these 17-keto steroids, the cyclopropyl ring eliminated product, androst-4-ene-3,17-dione (9), was isolated in 6, 4, and 8% yields, respectively. A cyclopropyl ring migration product, 6α,7α-cyclopropanoandrost-4-ene-3,17-dione (16), was isolated from the incubation mixture of 6 in 4% yield, also 10% yield of 16 was obtained when 5,6α-cyclopropano-5α-androst-7-ene-3,17-dione (12) was incubated. The cyclopropyl ring opening and subsequent reduction followed by oxidation of the two major biotransformation products, 5,6β-cyclopropano-5β-androsta-3,17-dione (10) and 5,6α-cyclopropano-5α-androsta-3,17-dione (7), gave 6β- and 6α-methylandrost-4-ene-3,17-dione in 60, and 45% yields, respectively. (C) 2000 Elsevier Science Inc.

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