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ethyl 6-(2-anilino-2-oxoethyl)-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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  • 913739-04-5 Structure
  • Basic information

    1. Product Name: ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate
    2. Synonyms: ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate
    3. CAS NO:913739-04-5
    4. Molecular Formula:
    5. Molecular Weight: 339.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 913739-04-5.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: ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate(913739-04-5)
    11. EPA Substance Registry System: ethyl 6-(2-anilino-2-oxoethyl)-1-benzothiophene-2-carboxylate(913739-04-5)
  • 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: 913739-04-5(Hazardous Substances Data)

913739-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913739-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,7,3 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 913739-04:
(8*9)+(7*1)+(6*3)+(5*7)+(4*3)+(3*9)+(2*0)+(1*4)=175
175 % 10 = 5
So 913739-04-5 is a valid CAS Registry Number.

913739-04-5Downstream Products

913739-04-5Relevant articles and documents

BENZOTHIOPHENE DERIVATIVES

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Page/Page column 81, (2008/06/13)

The present invention relates to a novel class of benzothiophene amide derivatives. The hydroxamic acid compounds can be used to treat cancer. The benzothiophene amide compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing terminal differentiation, and arresting cell growth and/or apoptosis of neoplastic cells, thereby inhibiting proliferation of such cells. Thus, the compounds of the present invention are useful in treating a patient having a tumor characterized by proliferation of neoplastic cells. The compounds of the invention may also be useful in the prevention and treatment of TRX-mediated diseases, such as autoimmune, allergic and inflammatory diseases, and in the prevention and/or treatment of diseases of the central nervous system (CNS), such as neurodegenerative diseases. The present invention further provides pharmaceutical compositions comprising the hydroxamic acid derivatives and safe dosing regimens of these pharmaceutical compositions, which are easy to follow, and which result in a therapeutically effective amount of the hydroxamic acid derivatives in vivo.

BENZOTHIOPHENE HYDROXAMIC ACID DERIVATIVES

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Page/Page column 50, (2008/06/13)

The present invention relates to a novel class of hydroxamic acid derivatives. The hydroxamic acid compounds can be used to treat cancer. The hydroxamic acid compounds can also inhibit histone deacetylase and are suitable for use in selectively inducing t

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