Cas 212072-22-5,4,6-Dichloro-3-[2-oxo-1-phenyl-pyrrolidin-(3E)-ylidenemethyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-2-carboxylic acid methyl ester

212072-22-5

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Basic information

Product Name: 4,6-Dichloro-3-[2-oxo-1-phenyl-pyrrolidin-(3E)-ylidenemethyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-2-carboxylic acid methyl ester
Synonyms: 4,6-Dichloro-3-[2-oxo-1-phenyl-pyrrolidin-(3E)-ylidenemethyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-2-carboxylic acid methyl ester
CAS NO:212072-22-5
Molecular Formula:
Molecular Weight: 545.538
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: 4,6-Dichloro-3-[2-oxo-1-phenyl-pyrrolidin-(3E)-ylidenemethyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4,6-Dichloro-3-[2-oxo-1-phenyl-pyrrolidin-(3E)-ylidenemethyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-2-carboxylic acid methyl ester(212072-22-5)
EPA Substance Registry System: 4,6-Dichloro-3-[2-oxo-1-phenyl-pyrrolidin-(3E)-ylidenemethyl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-indole-2-carboxylic acid methyl ester(212072-22-5)

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: 212072-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 212072-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,0,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 212072-22:
(8*2)+(7*1)+(6*2)+(5*0)+(4*7)+(3*2)+(2*2)+(1*2)=75
75 % 10 = 5
So 212072-22-5 is a valid CAS Registry Number.

212072-22-5Upstream product

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212072-22-5Relevant academic research and scientific papers

Unusual synthesis of new glycine antagonists via sequential aldol condensation-lactonization-elimination reaction

Giacobbe, Simone A.,Baraldi, Davide,Di Fabio, Romano

, p. 1689 - 1692 (2007/10/03)

Compounds 2 and 3 were designed in order to probe the North-East region of the strichnine-insensitive glycine binding site of the NMDA receptor. The two products were obtained readily by a tandem aldol condensation- lactonization-elimination step which af

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