Cas 246162-03-8,2-methyl-1,3-dioxo-6-(2-trimethylsilanyl-ethoxymethyl)-1,2,3,6-tetrahydro-pyrrolo[3,4-<i>c</i>]carbazole-4-carboxylic acid benzyl ester

246162-03-8

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Basic information

Product Name: 2-methyl-1,3-dioxo-6-(2-trimethylsilanyl-ethoxymethyl)-1,2,3,6-tetrahydro-pyrrolo[3,4-c]carbazole-4-carboxylic acid benzyl ester
Synonyms: 2-methyl-1,3-dioxo-6-(2-trimethylsilanyl-ethoxymethyl)-1,2,3,6-tetrahydro-pyrrolo[3,4-c]carbazole-4-carboxylic acid benzyl ester
CAS NO:246162-03-8
Molecular Formula:
Molecular Weight: 514.653
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: 2-methyl-1,3-dioxo-6-(2-trimethylsilanyl-ethoxymethyl)-1,2,3,6-tetrahydro-pyrrolo[3,4-c]carbazole-4-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-1,3-dioxo-6-(2-trimethylsilanyl-ethoxymethyl)-1,2,3,6-tetrahydro-pyrrolo[3,4-c]carbazole-4-carboxylic acid benzyl ester(246162-03-8)
EPA Substance Registry System: 2-methyl-1,3-dioxo-6-(2-trimethylsilanyl-ethoxymethyl)-1,2,3,6-tetrahydro-pyrrolo[3,4-c]carbazole-4-carboxylic acid benzyl ester(246162-03-8)

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: 246162-03-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 246162-03-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,1,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 246162-03:
(8*2)+(7*4)+(6*6)+(5*1)+(4*6)+(3*2)+(2*0)+(1*3)=118
118 % 10 = 8
So 246162-03-8 is a valid CAS Registry Number.

246162-03-8Upstream product

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246162-03-8Relevant academic research and scientific papers

A versatile new synthesis of 4-aryl- and heteroaryl-[3,4- c]pyrrolocarbazoles by [4+2] cycloaddition followed by palladium catalysed cross coupling

McCort, Gary,Duclos, Olivier,Cadilhac, Caroline,Guilpain, Eric

, p. 6211 - 6215 (2007/10/03)

4-Bromo- and 4-trifluorosulfonyloxypyrrolo[3,4-c]carbazoles were prepared in five steps via a [4+2] cycloaddition and were used as key intermediates in palladium-catalysed cross coupling reactions allowing the rapid generation of structurally diverse protein kinase C inhibitors.

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