Cas 104598-55-2,5,7-dihydroxy-6-<α-(2-hydroxy-6-isopropyltropon-3-yl)-4-methoxybenzyl>-2-phenyl-4H-chromen-4-one

104598-55-2

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Basic information

Product Name: 5,7-dihydroxy-6-<α-(2-hydroxy-6-isopropyltropon-3-yl)-4-methoxybenzyl>-2-phenyl-4H-chromen-4-one
Synonyms:
CAS NO:104598-55-2
Molecular Formula:
Molecular Weight: 536.581
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: 5,7-dihydroxy-6-<α-(2-hydroxy-6-isopropyltropon-3-yl)-4-methoxybenzyl>-2-phenyl-4H-chromen-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 5,7-dihydroxy-6-<α-(2-hydroxy-6-isopropyltropon-3-yl)-4-methoxybenzyl>-2-phenyl-4H-chromen-4-one(104598-55-2)
EPA Substance Registry System: 5,7-dihydroxy-6-<α-(2-hydroxy-6-isopropyltropon-3-yl)-4-methoxybenzyl>-2-phenyl-4H-chromen-4-one(104598-55-2)

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: 104598-55-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104598-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,9 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104598-55:
(8*1)+(7*0)+(6*4)+(5*5)+(4*9)+(3*8)+(2*5)+(1*5)=132
132 % 10 = 2
So 104598-55-2 is a valid CAS Registry Number.

104598-55-2Upstream product

104598-55-2Downstream Products

104598-55-2Relevant academic research and scientific papers

Synthesis and Antitumor Activity of Tropolone Derivatives. 4

Yamato, Masatoshi,Hashigaki, Kuniko,Sakai, Junko,Kawasaki, Youko,Tsukagoshi, Shigeru,Tashiro, Tazuko

, p. 117 - 120 (1987)

Modifications of monotropolone 2 having poor potency against P388 in mice were studied. The α-ethoxy group of 2, prepared from hinokitiol and benzaldehyde diethyl acetal, was replaced with a phenolic or heteroaromatic compound by heating 2 with the approp

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