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CAS

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154649-47-5

methyl 5-(1-hydroxyethyl)-1-benzothiophene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154649-47-5 Structure

  • Basic information

    1. Product Name: methyl 5-(1-hydroxyethyl)-1-benzothiophene-2-carboxylate
    2. Synonyms: Methyl-5-(1-hydroxyethyl)-1-benzothiophen-2-carboxylat
    3. CAS NO:154649-47-5
    4. Molecular Formula: C12H12O3S
    5. Molecular Weight: 236.2869
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154649-47-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 388°C at 760 mmHg
    3. Flash Point: 188.5°C
    4. Appearance: N/A
    5. Density: 1.298g/cm3
    6. Vapor Pressure: 1.02E-06mmHg at 25°C
    7. Refractive Index: 1.637
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: methyl 5-(1-hydroxyethyl)-1-benzothiophene-2-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 5-(1-hydroxyethyl)-1-benzothiophene-2-carboxylate(154649-47-5)
    12. EPA Substance Registry System: methyl 5-(1-hydroxyethyl)-1-benzothiophene-2-carboxylate(154649-47-5)

  • 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: 154649-47-5(Hazardous Substances Data)

154649-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154649-47-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,6,4 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 154649-47:
(8*1)+(7*5)+(6*4)+(5*6)+(4*4)+(3*9)+(2*4)+(1*7)=155
155 % 10 = 5
So 154649-47-5 is a valid CAS Registry Number.

154649-47-5Relevant articles and documents

UROKINASE INHIBITORS

-

, (2008/06/13)

Disclosed are benzothiophene and thienothiophene derivatives useful for inhibiting urokinase activity.

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