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744256-32-4

6-(4-methoxy-phenyl)-5-oxo-hexanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 744256-32-4 Structure

  • Basic information

    1. Product Name: 6-(4-methoxy-phenyl)-5-oxo-hexanenitrile
    2. Synonyms:
    3. CAS NO:744256-32-4
    4. Molecular Formula:
    5. Molecular Weight: 217.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 744256-32-4.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: 6-(4-methoxy-phenyl)-5-oxo-hexanenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(4-methoxy-phenyl)-5-oxo-hexanenitrile(744256-32-4)
    11. EPA Substance Registry System: 6-(4-methoxy-phenyl)-5-oxo-hexanenitrile(744256-32-4)

  • 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: 744256-32-4(Hazardous Substances Data)

744256-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 744256-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,2,5 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 744256-32:
(8*7)+(7*4)+(6*4)+(5*2)+(4*5)+(3*6)+(2*3)+(1*2)=164
164 % 10 = 4
So 744256-32-4 is a valid CAS Registry Number.

744256-32-4Relevant articles and documents

Estrogen receptor ligands. Part 5: The SAR of dihydrobenzoxathiins containing modified basic side chains

Tan, Qiang,Birzin, Elizabeth T.,Chan, Wanda,Yang, Yi Tien,Pai, Lee-Yuh,Hayes, Edward C.,Dasilva, Carolyn A.,DiNinno, Frank,Rohrer, Susan P.,Schaeffer, James M.,Hammond, Milton L.

, p. 3747 - 3751 (2004)

Dihydrobenzoxathiin analogs (1-11) with modifications on the basic side chain region were prepared and evaluated for estrogen/anti-estrogen activity in both in vitro and in vivo models. The compounds generally maintained a high degree of selectivity for ERα over ERβ, similar to the original lead compound I. Many of the compounds also maintained high potency in the inhibition of human carcinoma MCF-7 cell growth. However, all were less potent in the inhibition of estradiol-triggered uterine growth. This work demonstrates the sensitive nature of modification to the antagonist basic side chain region.

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