Cas 185540-12-9,1,8-Naphthyridine-3-carboxylic acid, 1,2-dihydro-4-(2-methoxyphenyl)-1-methyl-2-oxo-

185540-12-9

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Basic information

Product Name: 1,8-Naphthyridine-3-carboxylic acid, 1,2-dihydro-4-(2-methoxyphenyl)-1-methyl-2-oxo-
Synonyms:
CAS NO:185540-12-9
Molecular Formula: C17H14N2O4
Molecular Weight: 310.309
EINECS: N/A
Product Categories: N/A
Mol File: 185540-12-9.mol
Article Data: 2

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: 1,8-Naphthyridine-3-carboxylic acid, 1,2-dihydro-4-(2-methoxyphenyl)-1-methyl-2-oxo-(CAS DataBase Reference)
NIST Chemistry Reference: 1,8-Naphthyridine-3-carboxylic acid, 1,2-dihydro-4-(2-methoxyphenyl)-1-methyl-2-oxo-(185540-12-9)
EPA Substance Registry System: 1,8-Naphthyridine-3-carboxylic acid, 1,2-dihydro-4-(2-methoxyphenyl)-1-methyl-2-oxo-(185540-12-9)

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: 185540-12-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185540-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,5,4 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 185540-12:
(8*1)+(7*8)+(6*5)+(5*5)+(4*4)+(3*0)+(2*1)+(1*2)=139
139 % 10 = 9
So 185540-12-9 is a valid CAS Registry Number.

185540-12-9Upstream product

185540-12-9Downstream Products

185540-12-9Relevant articles and documents

Synthesis and structure-activity relationship studies on a novel series of naphthylidinoylureas as inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT)

Ohnuma, Satoshi,Muraoka, Masami,Ioriya, Katsuhisa,Ohashi, Naohito

, p. 1309 - 1311 (2007/10/03)

The synthesis and structure-activity relationships of N-phenyl-N′-[3- (4-phenylnaphthylidinoyl)]urea derivatives 3 as a novel structural class of potent ACAT inhibitors is described. A 3-methoxy group substituted on the naphthylidinone 4-phenyl ring, toge

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