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1036384-78-7

5-hydroxy-6-naphthalen-1-yl-1-phenyl-hexan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036384-78-7 Structure

  • Basic information

    1. Product Name: 5-hydroxy-6-naphthalen-1-yl-1-phenyl-hexan-3-one
    2. Synonyms: 5-hydroxy-6-naphthalen-1-yl-1-phenyl-hexan-3-one
    3. CAS NO:1036384-78-7
    4. Molecular Formula:
    5. Molecular Weight: 318.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036384-78-7.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: 5-hydroxy-6-naphthalen-1-yl-1-phenyl-hexan-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-hydroxy-6-naphthalen-1-yl-1-phenyl-hexan-3-one(1036384-78-7)
    11. EPA Substance Registry System: 5-hydroxy-6-naphthalen-1-yl-1-phenyl-hexan-3-one(1036384-78-7)

  • 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: 1036384-78-7(Hazardous Substances Data)

1036384-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036384-78-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,3,8 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1036384-78:
(9*1)+(8*0)+(7*3)+(6*6)+(5*3)+(4*8)+(3*4)+(2*7)+(1*8)=147
147 % 10 = 7
So 1036384-78-7 is a valid CAS Registry Number.

1036384-78-7Relevant articles and documents

NOVEL BETA-HYDROXYKETONES AND BETA-ALKOXYKETONES WITH ESTROGENIC ACTIVITY

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Page/Page column 21, (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.

Synthesis and evaluation of estrogen agonism of diaryl 4,5- dihydroisoxazoles, 3-hydroxyketones, 3-methoxyketones, and 1,3-diketones: A compound set forming a 4D molecular library

Pulkkinen, Juha T.,Honkakoski, Paavo,Per?kyl?, Mikael,Berczi, Istvan,Laatikainen, Reino

supporting information; experimental part, p. 3562 - 3571 (2009/04/06)

In this paper, the preparation and systematic evaluation of estrogen receptor α (ERα) and estrogen receptor β (ERβ) activities of some diaryl-1,3-diones and their synthetic intermediates, diaryl-4,5-dihydroisoxazoles, diaryl-3-hydroxyketones, diaryl-3-met

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