Cas 128832-34-8,DIETHYL 2-[(2-BENZOYL-4-CHLOROANILINO)METHYLENE]MALONATE

128832-34-8

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Basic information

Product Name: DIETHYL 2-[(2-BENZOYL-4-CHLOROANILINO)METHYLENE]MALONATE
Synonyms: DIETHYL 2-[(2-BENZOYL-4-CHLOROANILINO)METHYLENE]MALONATE;1,3-diethyl 2-{[(2-benzoyl-4-chlorophenyl)amino]methylidene}propanedioate
CAS NO:128832-34-8
Molecular Formula: C₂₁H₂₀ClNO₅
Molecular Weight: 401.84
EINECS: N/A
Product Categories: N/A
Mol File: 128832-34-8.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: DIETHYL 2-[(2-BENZOYL-4-CHLOROANILINO)METHYLENE]MALONATE(CAS DataBase Reference)
NIST Chemistry Reference: DIETHYL 2-[(2-BENZOYL-4-CHLOROANILINO)METHYLENE]MALONATE(128832-34-8)
EPA Substance Registry System: DIETHYL 2-[(2-BENZOYL-4-CHLOROANILINO)METHYLENE]MALONATE(128832-34-8)

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: 128832-34-8(Hazardous Substances Data)

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128832-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128832-34-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,3 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128832-34:
(8*1)+(7*2)+(6*8)+(5*8)+(4*3)+(3*2)+(2*3)+(1*4)=138
138 % 10 = 8
So 128832-34-8 is a valid CAS Registry Number.

128832-34-8Upstream product

128832-34-8Downstream Products

128832-35-9 6-Chloro-4-phenyl-3-quinolinecarboxylic acid ethyl ester

128832-34-8Relevant articles and documents

Novel Acyl-CoA:Cholesterol Acyltransferase Inhibitors. Synthesis and Biological Activity of 3-Quinolylurea Derivatives

Tawada, Hiroyuki,Harcourt, Myles,Kawamura, Noriaki,Kajino, Masahiro,Ishikawa, Eiichiro,et al.

, p. 2079 - 2084 (2007/10/02)

A series of 3-quinolylurea derivatives (1) was synthesized and evaluated for acyl-CoA:cholesterol acyltransferase (ACAT) inhibitory activity.For in vitro studies, the most potent inhibitory activity was found in derivatives having substituents at the 6,7-

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