Cas 1174889-32-7,3-[3-(4-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]-isoxazole-4,5-dicarboxylic acid diethyl ester

1174889-32-7

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Basic information

Product Name: 3-[3-(4-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]-isoxazole-4,5-dicarboxylic acid diethyl ester
Synonyms: 3-[3-(4-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]-isoxazole-4,5-dicarboxylic acid diethyl ester
CAS NO:1174889-32-7
Molecular Formula:
Molecular Weight: 510.344
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-[3-(4-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]-isoxazole-4,5-dicarboxylic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-[3-(4-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]-isoxazole-4,5-dicarboxylic acid diethyl ester(1174889-32-7)
EPA Substance Registry System: 3-[3-(4-bromophenyl)-1-phenyl-1H-pyrazol-4-yl]-isoxazole-4,5-dicarboxylic acid diethyl ester(1174889-32-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1174889-32-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174889-32-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,8,8 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1174889-32:
(9*1)+(8*1)+(7*7)+(6*4)+(5*8)+(4*8)+(3*9)+(2*3)+(1*2)=197
197 % 10 = 7
So 1174889-32-7 is a valid CAS Registry Number.

1174889-32-7Upstream product

762-21-0 acetylenedicarboxylic acid diethyl ester

1174889-32-7Downstream Products

1174889-32-7Relevant academic research and scientific papers

Synthesis and antinociceptive activity of pyrazolyl isoxazolines and pyrazolyl isoxazoles

Karthikeyan,Veenus Seelan,Lalitha,Perumal

, p. 3370 - 3373 (2009)

Pyrazolyl isoxazolines and isoxazoles were synthesised in moderate to good yields using 1,3-dipolar cycloaddition of pyrazole derived nitrile oxide with various dipolarophiles such as N-substituted maleimide, diethylacetylene dicarboxylate and phenylacety

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