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5-naphthalen-1-yl-3-phenethyl-4,5-dihydroisoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036384-74-3 Structure
  • Basic information

    1. Product Name: 5-naphthalen-1-yl-3-phenethyl-4,5-dihydroisoxazole
    2. Synonyms: 5-naphthalen-1-yl-3-phenethyl-4,5-dihydroisoxazole
    3. CAS NO:1036384-74-3
    4. Molecular Formula:
    5. Molecular Weight: 315.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036384-74-3.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-naphthalen-1-yl-3-phenethyl-4,5-dihydroisoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-naphthalen-1-yl-3-phenethyl-4,5-dihydroisoxazole(1036384-74-3)
    11. EPA Substance Registry System: 5-naphthalen-1-yl-3-phenethyl-4,5-dihydroisoxazole(1036384-74-3)
  • 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: 1036384-74-3(Hazardous Substances Data)

1036384-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036384-74-3 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 1036384-74:
(9*1)+(8*0)+(7*3)+(6*6)+(5*3)+(4*8)+(3*4)+(2*7)+(1*4)=143
143 % 10 = 3
So 1036384-74-3 is a valid CAS Registry Number.

1036384-74-3Relevant articles and documents

NOVEL 4,5-DIHYDROISOXAZOLES WITH ESTROGENIC ACTIVITY

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Page/Page column 11; 34-35, (2009/06/27)

This invention relates to novel 4,5-dihydroisoxazoles of formula (I), to their use as estrogen receptor modulators, and to methods of 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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