Cas 496955-95-4,1H-Indole-2-carboxylic acid, 4,6-dichloro-3-[(2,4-dioxo-3-phenyl-1-imidazolidinyl)methyl]-, ethyl ester

496955-95-4

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Basic information

Product Name: 1H-Indole-2-carboxylic acid, 4,6-dichloro-3-[(2,4-dioxo-3-phenyl-1-imidazolidinyl)methyl]-, ethyl ester
Synonyms:
CAS NO:496955-95-4
Molecular Formula: C21H17Cl2N3O4
Molecular Weight: 446.29
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: 1H-Indole-2-carboxylic acid, 4,6-dichloro-3-[(2,4-dioxo-3-phenyl-1-imidazolidinyl)methyl]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indole-2-carboxylic acid, 4,6-dichloro-3-[(2,4-dioxo-3-phenyl-1-imidazolidinyl)methyl]-, ethyl ester(496955-95-4)
EPA Substance Registry System: 1H-Indole-2-carboxylic acid, 4,6-dichloro-3-[(2,4-dioxo-3-phenyl-1-imidazolidinyl)methyl]-, ethyl ester(496955-95-4)

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: 496955-95-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 496955-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,9,5 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 496955-95:
(8*4)+(7*9)+(6*6)+(5*9)+(4*5)+(3*5)+(2*9)+(1*5)=234
234 % 10 = 4
So 496955-95-4 is a valid CAS Registry Number.

496955-95-4Upstream product

496955-95-4Downstream Products

496955-95-4Relevant academic research and scientific papers

Hydantoin-substituted 4,6-dichloroindole-2-carboxylic acids as ligands with high affinity for the glycine binding site of the NMDA receptor

Jansen, Michaela,Potschka, Heidrun,Brand, Claudia,L?scher, Wolfgang,Dannhardt, Gerd

, p. 64 - 73 (2007/10/03)

A novel series of C-3 substituted 4,6-dichloroindole-2-carboxylic acids was synthesized to investigate the influence of different hydrogen-bond donor and acceptor groups at this specific position on the affinity to the glycine site of the NMDA receptor. T

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