Cas 189124-63-8,2H-Benz[e]isoindole-3-carboxylic acid, 1-[[5-[(1,1-dimethylethoxy)carbonyl]-3-ethyl-4-methyl-1H-pyrrol-2-yl]meth yl]-6-nitro-, 1,1-dimethylethyl ester

189124-63-8

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Basic information

Product Name: 2H-Benz[e]isoindole-3-carboxylic acid, 1-[[5-[(1,1-dimethylethoxy)carbonyl]-3-ethyl-4-methyl-1H-pyrrol-2-yl]meth yl]-6-nitro-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:189124-63-8
Molecular Formula: C30H35N3O6
Molecular Weight:
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: 2H-Benz[e]isoindole-3-carboxylic acid, 1-[[5-[(1,1-dimethylethoxy)carbonyl]-3-ethyl-4-methyl-1H-pyrrol-2-yl]meth yl]-6-nitro-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2H-Benz[e]isoindole-3-carboxylic acid, 1-[[5-[(1,1-dimethylethoxy)carbonyl]-3-ethyl-4-methyl-1H-pyrrol-2-yl]meth yl]-6-nitro-, 1,1-dimethylethyl ester(189124-63-8)
EPA Substance Registry System: 2H-Benz[e]isoindole-3-carboxylic acid, 1-[[5-[(1,1-dimethylethoxy)carbonyl]-3-ethyl-4-methyl-1H-pyrrol-2-yl]meth yl]-6-nitro-, 1,1-dimethylethyl ester(189124-63-8)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 189124-63-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 189124-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,1,2 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 189124-63:
(8*1)+(7*8)+(6*9)+(5*1)+(4*2)+(3*4)+(2*6)+(1*3)=158
158 % 10 = 8
So 189124-63-8 is a valid CAS Registry Number.

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189124-63-8Relevant academic research and scientific papers

Synthesis of novel porphyrin chromophores from nitroarenes: Further applications of the Barton-Zard pyrrole condensation

Lash, Timothy D.,Wijesinghe, Chaminda,Osuma, Augustine T.,Patel, Jyoti R.

, p. 2031 - 2034 (1997)

Porphyrins with fused nitronaphthalene and benzothiadiazole subunits have been synthesized by the '2 + 2' and '3 + 1' methodologies; the key pyrrolic intermediates were prepared by the base catalyzed condensation of dinitronaphthalenes or 4-nitro-2,1,3-benzothiadiazole with isocyanoacetates.

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