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3-[3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl]-2-phenyl-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1392103-82-0 Structure
  • Basic information

    1. Product Name: 3-[3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl]-2-phenyl-1H-indole
    2. Synonyms: 3-[3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl]-2-phenyl-1H-indole
    3. CAS NO:1392103-82-0
    4. Molecular Formula:
    5. Molecular Weight: 372.854
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1392103-82-0.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: 3-[3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl]-2-phenyl-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl]-2-phenyl-1H-indole(1392103-82-0)
    11. EPA Substance Registry System: 3-[3-(4-chlorophenyl)-4,5-dihydroisoxazol-5-yl]-2-phenyl-1H-indole(1392103-82-0)
  • 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: 1392103-82-0(Hazardous Substances Data)

1392103-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392103-82-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,1,0 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1392103-82:
(9*1)+(8*3)+(7*9)+(6*2)+(5*1)+(4*0)+(3*3)+(2*8)+(1*2)=140
140 % 10 = 0
So 1392103-82-0 is a valid CAS Registry Number.

1392103-82-0Downstream Products

1392103-82-0Relevant articles and documents

Synthesis and biological evaluation of novel indolyl isoxazoline derivatives as analgesic and antiinflammatory agents

Chavan,Khadke

experimental part, p. 2711 - 2716 (2012/09/10)

A series of 3-(2-(4-substituted phenyl)-1H-indol-3-yl)-1-(4-substituted phenyl)prop-2-en-1-one 3(a-l) were synthesized from substituted indole aldehydes. Using hydroxylamine hydrochloride the chalcones 3(a-l) were cyclized to afford a novel series of 2-(4-substituted phenyl)-3-(3-(4-substituted phenyl)-4,5-dihydroisoxazol-5-yl)-1H-indole 4(a-l). The structure of all these compounds were established on the basis of spectral (IR, 1H NMR) studies. The compounds 4(a-l) were evaluated for the antiinflammatory and analgesic activity by using different pharmacological models. The most active compounds were subjected to acute ulcerogenesis activity and were found to be less ulcerogenic than the reference drug indomethacin.

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