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849518-85-0

2-(thiophen-3-yl)butanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 849518-85-0 Structure

  • Basic information

    1. Product Name: 2-(thiophen-3-yl)butanenitrile
    2. Synonyms: 2-(thiophen-3-yl)butanenitrile
    3. CAS NO:849518-85-0
    4. Molecular Formula: C8H9NS
    5. Molecular Weight: 151.22876
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 849518-85-0.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: 2-(thiophen-3-yl)butanenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(thiophen-3-yl)butanenitrile(849518-85-0)
    11. EPA Substance Registry System: 2-(thiophen-3-yl)butanenitrile(849518-85-0)

  • 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: 849518-85-0(Hazardous Substances Data)

849518-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849518-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,5,1 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849518-85:
(8*8)+(7*4)+(6*9)+(5*5)+(4*1)+(3*8)+(2*8)+(1*5)=220
220 % 10 = 0
So 849518-85-0 is a valid CAS Registry Number.

849518-85-0Downstream Products

849518-85-0Relevant articles and documents

PYRAZOLOPYRIDINES

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Page/Page column 58, (2010/11/18)

The present invention relates to compounds useful as inhibitors of protein kinase. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders. The invention also provides processes for preparing compounds of the inventions.

Nucleophile-catalyzed asymmetric acylations of silyl ketene imines: Application to the enantioselective synthesis of verapamil

Mermerian, Ara H.,Fu, Gregory C.

, p. 949 - 952 (2007/10/03)

All-carbon quaternary stereocenters are generated with good enantioselectivity through a nucleophile-catalyzed acylation reaction of silyl ketene imines (see scheme, TBS = tert-butyldimethylsilyl). The method is applied to the first catalytic asymmetric synthesis of the drug verapamil.

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