Cas 850035-72-2,2-Propen-1-one, 3-(dimethylamino)-1-(2-naphthalenyl)-2-(3,4,5-trimethoxyphenyl)-

850035-72-2

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Basic information

Product Name: 2-Propen-1-one, 3-(dimethylamino)-1-(2-naphthalenyl)-2-(3,4,5-trimethoxyphenyl)-
Synonyms:
CAS NO:850035-72-2
Molecular Formula: C24H25NO4
Molecular Weight: 391.467
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: 2-Propen-1-one, 3-(dimethylamino)-1-(2-naphthalenyl)-2-(3,4,5-trimethoxyphenyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propen-1-one, 3-(dimethylamino)-1-(2-naphthalenyl)-2-(3,4,5-trimethoxyphenyl)-(850035-72-2)
EPA Substance Registry System: 2-Propen-1-one, 3-(dimethylamino)-1-(2-naphthalenyl)-2-(3,4,5-trimethoxyphenyl)-(850035-72-2)

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: 850035-72-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 850035-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,0,3 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850035-72:
(8*8)+(7*5)+(6*0)+(5*0)+(4*3)+(3*5)+(2*7)+(1*2)=142
142 % 10 = 2
So 850035-72-2 is a valid CAS Registry Number.

850035-72-2Upstream product

4637-24-5 N,N-dimethyl-formamide dimethyl acetal

850035-72-2Downstream Products

850035-72-2Relevant academic research and scientific papers

New naphthylcombretastatins. Modifications on the ethylene bridge

Sanchez Maya, Ana B.,Perez-Melero, Concepcion,Salvador, Nelida,Pelaez, Rafael,Caballero, Esther,Medarde, Manuel

, p. 2097 - 2107 (2005)

Compounds with three aromatic systems, carrying a 2-naphthalene and a 3,4,5-trimethoxyphenyl moieties bonded to five-membered, six-membered or fused heterocycles display potent cytotoxic effect and inhibition of tubulin polymerization, in agreement with t

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