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146137-94-2

6-IODO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146137-94-2 Structure

  • Basic information

    1. Product Name: 6-IODO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
    2. Synonyms: 6-IODO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER
    3. CAS NO:146137-94-2
    4. Molecular Formula: C10H7 I O2 S
    5. Molecular Weight: 318.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146137-94-2.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: 6-IODO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-IODO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER(146137-94-2)
    11. EPA Substance Registry System: 6-IODO-BENZO[B]THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER(146137-94-2)

  • 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: 146137-94-2(Hazardous Substances Data)

146137-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146137-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,3 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 146137-94:
(8*1)+(7*4)+(6*6)+(5*1)+(4*3)+(3*7)+(2*9)+(1*4)=132
132 % 10 = 2
So 146137-94-2 is a valid CAS Registry Number.

146137-94-2Downstream Products

146137-94-2Relevant articles and documents

UROKINASE INHIBITORS

-

, (2008/06/13)

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

Fluorine as an ortho-directing group in aromatic metalation: A two step preparation of substituted benzo[b] thiophene-2-carboxylates

Bridges, Alexander J.,Lee, Arthur,Maduakor, Emmanuel C.,Eric Schwartz

, p. 7499 - 7502 (2007/10/02)

A simple 2-step synthesis of B-ring substituted benzo[b]thiophene-2-carboxylates from aryl fluorides has been developed. The route involves a selective lithiation ortho to fluorine, followed by formylation, and subsequently, displacement of fluorine with

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