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108516-23-0

[α-2H]cyclopentyl phenyl ketone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108516-23-0 Structure

  • Basic information

    1. Product Name: [α-2H]cyclopentyl phenyl ketone
    2. Synonyms: [α-2H]cyclopentyl phenyl ketone
    3. CAS NO:108516-23-0
    4. Molecular Formula:
    5. Molecular Weight: 175.235
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108516-23-0.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: [α-2H]cyclopentyl phenyl ketone(CAS DataBase Reference)
    10. NIST Chemistry Reference: [α-2H]cyclopentyl phenyl ketone(108516-23-0)
    11. EPA Substance Registry System: [α-2H]cyclopentyl phenyl ketone(108516-23-0)

  • 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: 108516-23-0(Hazardous Substances Data)

108516-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108516-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,1 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108516-23:
(8*1)+(7*0)+(6*8)+(5*5)+(4*1)+(3*6)+(2*2)+(1*3)=110
110 % 10 = 0
So 108516-23-0 is a valid CAS Registry Number.

108516-23-0Downstream Products

108516-23-0Relevant articles and documents

Investigations into the C-deuteriation of aryl alkyl ketones using urea as a pro-base in the presence of a deuterium donor

Coumbarides, Gregory S.,Eames, Jason,Suggate, Michael J.,Weerasooriya, Neluka

, p. 641 - 652 (2006)

Results are reported on the regioselective C-deuteriation of a series of enolates derived from the deprotonation of aryl alkyl ketones using dilithiated urea as the pro-base in the presence of a suitable deuterium donor. Copyright

Catalytic asymmetric synthesis of (S)-oxybutynin and a versatile intermediate for antimuscarinic agents

Masumoto, Shuji,Suzuki, Masato,Kanai, Motomu,Shibasaki, Masakatsu

, p. 10497 - 10504 (2007/10/03)

A practical synthesis of (S)-oxybutynin, a muscarinic receptor antagonist, using catalytic enantioselective cyanosilylation of cyclohexyl phenyl ketone (9a) as a key step is described. The key reaction proceeded with 94% ee using 1 mol% of Gd-1 catalyst,

Investigations into the regioselective C-deuteration of acyclic and exocyclic enolates

Eames, Jason,Coumbarides, Gregory S.,Suggate, Michael J.,Weerasooriya, Neluka

, p. 634 - 641 (2007/10/03)

Results are reported on the regioselective C-deuteration of a series of related acyclic and exocyclic enolates derived from substituted aryl ketones. We comment on factors, such as the presence of additives and the structural nature of the enolate, that influence the observed C-deuteration and discuss the role of the deuterium donor. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).

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