Cas 143772-66-1,Pyrrolo[3,2-b]carbazole-2-carboxylic acid, 8-fluoro-1,5-dihydro-3,4-dimethyl-, phenylmethyl ester

143772-66-1

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Basic information

Product Name: Pyrrolo[3,2-b]carbazole-2-carboxylic acid, 8-fluoro-1,5-dihydro-3,4-dimethyl-, phenylmethyl ester
Synonyms:
CAS NO:143772-66-1
Molecular Formula: C24H19FN2O2
Molecular Weight: 386.425
EINECS: N/A
Product Categories: N/A
Mol File: 143772-66-1.mol
Article Data: 1

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: Pyrrolo[3,2-b]carbazole-2-carboxylic acid, 8-fluoro-1,5-dihydro-3,4-dimethyl-, phenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Pyrrolo[3,2-b]carbazole-2-carboxylic acid, 8-fluoro-1,5-dihydro-3,4-dimethyl-, phenylmethyl ester(143772-66-1)
EPA Substance Registry System: Pyrrolo[3,2-b]carbazole-2-carboxylic acid, 8-fluoro-1,5-dihydro-3,4-dimethyl-, phenylmethyl ester(143772-66-1)

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: 143772-66-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143772-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,7 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143772-66:
(8*1)+(7*4)+(6*3)+(5*7)+(4*7)+(3*2)+(2*6)+(1*6)=141
141 % 10 = 1
So 143772-66-1 is a valid CAS Registry Number.

143772-66-1Upstream product

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143772-66-1Relevant articles and documents

A New Synthetic Route to Pyrrolocarbazoles, 1H-Benzofuroindoles and 1H-Benzothienoindoles

Chunchatprasert, Laddawan,Rao, K. R. Nagaraja,Shannon, Patrick V. R.

, p. 1779 - 1784 (2007/10/02)

The heterocyclic systems pyrrolocarbazole, 1H-benzofuroindole and 1H-benzothienoindole were synthesized by Montmorillonite K10 clay-catalysed condensation of 5-acetoxymethyl-4-acetylpyrroles with various indoles, benzofuran and ben

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