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335421-55-1

Cyclopentanecarbonitrile, 2-oxo-1-(3-oxopentyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 335421-55-1 Structure

  • Basic information

    1. Product Name: Cyclopentanecarbonitrile, 2-oxo-1-(3-oxopentyl)- (9CI)
    2. Synonyms: Cyclopentanecarbonitrile, 2-oxo-1-(3-oxopentyl)- (9CI)
    3. CAS NO:335421-55-1
    4. Molecular Formula: C11H15NO2
    5. Molecular Weight: 193.2423
    6. EINECS: N/A
    7. Product Categories: CYCLOPENTANE
    8. Mol File: 335421-55-1.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: Cyclopentanecarbonitrile, 2-oxo-1-(3-oxopentyl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclopentanecarbonitrile, 2-oxo-1-(3-oxopentyl)- (9CI)(335421-55-1)
    11. EPA Substance Registry System: Cyclopentanecarbonitrile, 2-oxo-1-(3-oxopentyl)- (9CI)(335421-55-1)

  • 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: 335421-55-1(Hazardous Substances Data)

335421-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335421-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,4,2 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 335421-55:
(8*3)+(7*3)+(6*5)+(5*4)+(4*2)+(3*1)+(2*5)+(1*5)=121
121 % 10 = 1
So 335421-55-1 is a valid CAS Registry Number.

335421-55-1Relevant articles and documents

A modified Robinson annulation process to α,α-disubstituted-β,γ-unsaturated cyclohexanone system. Application to the total synthesis of nanaimoal

Liu, Hsing-Jang,Ly, Tai Wei,Tai, Chia-Liang,Wu, Jen-Dar,Liang, Jinn-Kwei,Guo, Jiunn-Cheh,Tseng, Nai-Wen,Shia, Kak-Shan

, p. 1209 - 1226 (2007/10/03)

4-Cyano-2-cyclohexenones were found to be susceptible to reductive alkylation reactions, giving the corresponding 2,2-disubstituted-3-cyclohexenone derivatives in a completely regioselective manner. This newly developed methodology has been successfully applied towards the total synthesis, in racemic form, of the marine natural product nanaimoal.

Reductive alkylation of γ-cyano-α,β-unsaturated ketones. A modified Robinson annulation process to α,α-disubstituted-β,γ-unsaturated cyclohexanone system

Tai,Tai Wei Ly,Wu,Shia,Liu

, p. 214 - 217 (2007/10/03)

Reductive alkylation of various 4-cyano-2-cyclohexenones, readily available from α-cyano ketones via a Robinson annulation process, gave rise to the corresponding 2,2-disubstituted-3-cyclohexenone derivatives in a completely regioselective manner. Application of this methodology resulted in an efficient synthesis of the marine natural product nanaimoal in racemic form.

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