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1158956-44-5

4-(4-methoxyphenyl-1-yl)-3-hydroxy-1-(4-methoxyphenyl)-1-butanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1158956-44-5 Structure

  • Basic information

    1. Product Name: 4-(4-methoxyphenyl-1-yl)-3-hydroxy-1-(4-methoxyphenyl)-1-butanone
    2. Synonyms: 4-(4-methoxyphenyl-1-yl)-3-hydroxy-1-(4-methoxyphenyl)-1-butanone
    3. CAS NO:1158956-44-5
    4. Molecular Formula:
    5. Molecular Weight: 300.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1158956-44-5.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: 4-(4-methoxyphenyl-1-yl)-3-hydroxy-1-(4-methoxyphenyl)-1-butanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-methoxyphenyl-1-yl)-3-hydroxy-1-(4-methoxyphenyl)-1-butanone(1158956-44-5)
    11. EPA Substance Registry System: 4-(4-methoxyphenyl-1-yl)-3-hydroxy-1-(4-methoxyphenyl)-1-butanone(1158956-44-5)

  • 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: 1158956-44-5(Hazardous Substances Data)

1158956-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158956-44-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,9,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1158956-44:
(9*1)+(8*1)+(7*5)+(6*8)+(5*9)+(4*5)+(3*6)+(2*4)+(1*4)=195
195 % 10 = 5
So 1158956-44-5 is a valid CAS Registry Number.

1158956-44-5Downstream Products

1158956-44-5Relevant articles and documents

Facile Synthesis of Natural Alkoxynaphthalene Analogues from Plant Alkoxybenzenes

Tsyganov, Dmitry V.,Krayushkin, Mikhail M.,Konyushkin, Leonid D.,Strelenko, Yuri A.,Semenova, Marina N.,Semenov, Victor V.

, p. 923 - 928 (2016)

Analogues of the bioactive natural alkoxynaphthalene pycnanthulignene D were synthesized by an efficient method. The starting plant allylalkoxybenzenes (1) are easily available from the plant essential oils of sassafras, dill, and parsley. The target 1-arylalkoxynaphthalenes (5) exhibited antiproliferative activity in a phenotypic sea urchin embryo assay.

NOVEL BETA-HYDROXYKETONES AND BETA-ALKOXYKETONES WITH ESTROGENIC ACTIVITY

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Page/Page column 15, (2009/06/27)

This invention relates to β-hydroxyketones and β-alkoxyketones of formula (I), to their use as estrogen receptor modulators, and to methods for their preparation.

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