Cas 71088-29-4,4-methoxy-<i>N</i>-(1-phenyl-4,5-dihydro-1<i>H</i>-pyrazol-3-yl)-benzamide

71088-29-4

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Basic information

Product Name: 4-methoxy-N-(1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-benzamide
Synonyms: 4-methoxy-N-(1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-benzamide
CAS NO:71088-29-4
Molecular Formula:
Molecular Weight: 295.341
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: 4-methoxy-N-(1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methoxy-N-(1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-benzamide(71088-29-4)
EPA Substance Registry System: 4-methoxy-N-(1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-benzamide(71088-29-4)

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: 71088-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71088-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,8 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71088-29:
(7*7)+(6*1)+(5*0)+(4*8)+(3*8)+(2*2)+(1*9)=124
124 % 10 = 4
So 71088-29-4 is a valid CAS Registry Number.

71088-29-4Upstream product

3314-35-0 3-Amino-1-phenyl-2-pyrazoline

71088-29-4Downstream Products

71088-29-4Relevant academic research and scientific papers

Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists

Van Muijlwijk-Koezen,Timmerman,Vollinga,Frijtag von Drabbe Künzel,De Groote,Visser,IJzerman

, p. 749 - 762 (2007/10/03)

Novel classes of heterocyclic compounds as adenosine antagonists were developed based on a template approach. Structure-affinity relationships revealed insights for extended knowledge of the receptor-ligand interaction. We replaced the bicyclic heterocycl

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