Cas 1382626-75-6,8-(4,5-dihydro-5-(3-nitrophenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one

1382626-75-6

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Basic information

Product Name: 8-(4,5-dihydro-5-(3-nitrophenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one
Synonyms: 8-(4,5-dihydro-5-(3-nitrophenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one
CAS NO:1382626-75-6
Molecular Formula:
Molecular Weight: 365.345
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: 8-(4,5-dihydro-5-(3-nitrophenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 8-(4,5-dihydro-5-(3-nitrophenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one(1382626-75-6)
EPA Substance Registry System: 8-(4,5-dihydro-5-(3-nitrophenyl)-1H-pyrazol-3-yl)-7-hydroxy-4-methyl-2H-1-benzopyran-2-one(1382626-75-6)

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: 1382626-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1382626-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,2,6,2 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1382626-75:
(9*1)+(8*3)+(7*8)+(6*2)+(5*6)+(4*2)+(3*6)+(2*7)+(1*5)=176
176 % 10 = 6
So 1382626-75-6 is a valid CAS Registry Number.

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1382626-75-6Relevant academic research and scientific papers

Synthesis of 4-methylcoumarin derivatives containing 4,5-dihydropyrazole moiety to scavenge radicals and to protect DNA

Xiao, Chuan,Luo, Xu-Yang,Li, De-Jun,Lu, Hang,Liu, Zai-Qun,Song, Zhi-Guang,Jin, Ying-Hua

, p. 159 - 167 (2012)

A series of 4-methylcoumarin derivatives containing 4,5-dihydropyrazole moiety were synthesized and their antioxidant activities were evaluated in AAPH (2,2′-azobis(2-amidinopropane hydrochloride))-induced oxidation of DNA, and in trapping DPPH (2,2′-diph

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