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1196873-49-0

2-(5-(trimethylsilyl)furan-2-yl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1196873-49-0 Structure

  • Basic information

    1. Product Name: 2-(5-(trimethylsilyl)furan-2-yl)ethanol
    2. Synonyms: 2-(5-(trimethylsilyl)furan-2-yl)ethanol
    3. CAS NO:1196873-49-0
    4. Molecular Formula:
    5. Molecular Weight: 184.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1196873-49-0.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: 2-(5-(trimethylsilyl)furan-2-yl)ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(5-(trimethylsilyl)furan-2-yl)ethanol(1196873-49-0)
    11. EPA Substance Registry System: 2-(5-(trimethylsilyl)furan-2-yl)ethanol(1196873-49-0)

  • 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: 1196873-49-0(Hazardous Substances Data)

1196873-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1196873-49-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,8,7 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1196873-49:
(9*1)+(8*1)+(7*9)+(6*6)+(5*8)+(4*7)+(3*3)+(2*4)+(1*9)=210
210 % 10 = 0
So 1196873-49-0 is a valid CAS Registry Number.

1196873-49-0Relevant articles and documents

HETEROCYCLIC AMIDES AS ROCK INHIBITORS

-

Page/Page column 81, (2011/10/03)

The present invention relates to new kinase inhibitors of formula (I), more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the application to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic diseases and Respiratory diseases.

Gold catalysis: benzanellation versus alkylidenecyclopentenone synthesis

Hashmi, A. Stephen K.,W?lfle, Michael

experimental part, p. 9021 - 9029 (2009/12/08)

A series of different furan-yn-ols were prepared by a three-step sequence. Their reaction with Gagosz's catalyst Ph3PAuNTf2 depends strongly on the substitution pattern of the substrate and the quality of the leaving group. Benzofurans, alkylidenecyclopentenones or Meyer-Schuster type products can be obtained. Improving the leaving group quality leads to the preferred formation of benzofurans.

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