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CAS

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148364-28-7

3-phenylcholest-5-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148364-28-7 Structure

  • Basic information

    1. Product Name: 3-phenylcholest-5-ene
    2. Synonyms: 3-phenylcholest-5-ene
    3. CAS NO:148364-28-7
    4. Molecular Formula:
    5. Molecular Weight: 446.76
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148364-28-7.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: 3-phenylcholest-5-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenylcholest-5-ene(148364-28-7)
    11. EPA Substance Registry System: 3-phenylcholest-5-ene(148364-28-7)

  • 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: 148364-28-7(Hazardous Substances Data)

148364-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148364-28-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,3,6 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 148364-28:
(8*1)+(7*4)+(6*8)+(5*3)+(4*6)+(3*4)+(2*2)+(1*8)=147
147 % 10 = 7
So 148364-28-7 is a valid CAS Registry Number.

148364-28-7Downstream Products

148364-28-7Relevant articles and documents

Montmorillonite clay catalysis. Part 8. Synthesis of arylcholestenes by Friedel-Crafts reaction catalysed by montmorillonite K-10

Li, Li-Jun,Lu, Bo,Li, Tong-Shuang,Li, Ji-Tai

, p. 1439 - 1449 (1998)

A series of 3β-arylcholestenes were synthesised by Friedel-Crafts reaction of cholesterol with arenes catalysed by montmorillonite K-10.

Cross-coupling of nonactivated primary and secondary alkyl halides with aryl Grignard reagents catalyzed by chiral iron pincer complexes

Bauer, Gerald,Cheung, Chi Wai,Hu, Xile

, p. 1726 - 1732 (2015/06/16)

Iron(III) bisoxazolinylphenylamido (bopa) pincer complexes are efficient precatalysts for the cross-coupling of nonactivated primary and secondary alkyl halides with phenyl Grignard reagents. The reactions proceed at room temperature in moderate to excellent yields. A variety of functional groups can be tolerated. The enantioselectivity of the coupling of secondary alkyl halides is low.

Synthesis of alkylbenzenes by Friedl-Crafts reactions catalysed by K10-montmorillonite

Sieskind,Albrecht

, p. 1197 - 1200 (2007/10/02)

Monoalkylation of benzene with primary, secondary and tertiary alcohols took place in high yields when K10-montmorillonite was used as acidic catalyst. Unexpected formation of 1-phenylalkylbenzenes occurred, beside other isomers with primary alcohols. Mon

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