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CAS

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16020-97-6

3,3-diphenylcyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16020-97-6 Structure

  • Basic information

    1. Product Name: 3,3-diphenylcyclopentanone
    2. Synonyms: 3,3-diphenylcyclopentanone
    3. CAS NO:16020-97-6
    4. Molecular Formula:
    5. Molecular Weight: 236.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16020-97-6.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: 3,3-diphenylcyclopentanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3-diphenylcyclopentanone(16020-97-6)
    11. EPA Substance Registry System: 3,3-diphenylcyclopentanone(16020-97-6)

  • 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: 16020-97-6(Hazardous Substances Data)

16020-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16020-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16020-97:
(7*1)+(6*6)+(5*0)+(4*2)+(3*0)+(2*9)+(1*7)=76
76 % 10 = 6
So 16020-97-6 is a valid CAS Registry Number.

16020-97-6Relevant articles and documents

Catalytic and regioselective ring expansion of arylcyclobutanones with trimethylsilyldiazomethane. Ligand-dependent entry to β-ketosilane or enolsilane adducts

Dabrowski, Jennifer A.,Moebius, David C.,Wommack, Andrew J.,Kornahrens, Anne F.,Kingsbury, Jason S.

supporting information; experimental part, p. 3598 - 3601 (2010/11/04)

Divergent reactivity is uncovered in the homologation of arylcyclobutanones with trimethylsilyldiazomethane. With Sc(OTf)3 as catalyst, enolsilanes are obtained with a high preference for methylene migration. By contrast, Sc(hfac)3 g

Metal mediated one-pot synthesis of cyclopentanones from allyl vinyl esters or diallyl ethers via tandem Claisen rearrangement and hydroacylation

Eilbracht,Gersmeier,Lennartz,Huber

, p. 330 - 334 (2007/10/02)

Cyclopentanones 3 and 7 are generated in a one-pot procedure from allyl vinyl ethers 1 and diallyl ethers 4, respectively. The conversion is carried out in the presence of RhCl(cod)(dppe) or RuCl2(PPh3)3 at elevated temper

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