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ethyl 4-phenyl-2-(phenylethynyl)thiophene-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384579-46-7 Structure
  • Basic information

    1. Product Name: ethyl 4-phenyl-2-(phenylethynyl)thiophene-3-carboxylate
    2. Synonyms: ethyl 4-phenyl-2-(phenylethynyl)thiophene-3-carboxylate
    3. CAS NO:1384579-46-7
    4. Molecular Formula:
    5. Molecular Weight: 332.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384579-46-7.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 4-phenyl-2-(phenylethynyl)thiophene-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4-phenyl-2-(phenylethynyl)thiophene-3-carboxylate(1384579-46-7)
    11. EPA Substance Registry System: ethyl 4-phenyl-2-(phenylethynyl)thiophene-3-carboxylate(1384579-46-7)
  • 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: 1384579-46-7(Hazardous Substances Data)

1384579-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384579-46-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,5,7 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1384579-46:
(9*1)+(8*3)+(7*8)+(6*4)+(5*5)+(4*7)+(3*9)+(2*4)+(1*6)=207
207 % 10 = 7
So 1384579-46-7 is a valid CAS Registry Number.

1384579-46-7Downstream Products

1384579-46-7Relevant articles and documents

Thieno[3,2-c]pyran-4-one based novel small molecules: Their synthesis, crystal structure analysis and in vitro evaluation as potential anticancer agents

Nakhi, Ali,Adepu, Raju,Rambabu,Kishore, Ravada,Vanaja,Kalle, Arunasree M.,Pal, Manojit

, p. 4418 - 4427 (2012/09/07)

Novel thieno[3,2-c]pyran-4-one based small molecules were designed as potential anticancer agents. Expeditious synthesis of these compounds was carried out via a multi-step sequence consisting of few steps such as Gewald reaction, Sandmeyer type iodination, Sonogashira type coupling followed by iodocyclization and then Pd-mediated various C-C bond forming reactions. The overall strategy involved the construction of thiophene ring followed by the fused pyranone moiety and then functionalization at C-7 position of the resultant thieno[3,2-c]pyran-4-one framework. Some of the compounds synthesized showed selective growth inhibition of cancer cells in vitro among which two compounds for example, 5d and 6c showed IC50 values in the range of 2.0-2.5 μM. The crystal structure analysis of an active compound along with hydrogen bonding patterns and molecular arrangement present within the molecule is described.

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