Cas 1401419-81-5,9-phenylsulfonyl-2-(1-phenylsulfonyl-2-methyl-1H-indol-3-yl)-3-nitro-9H-carbazole

1401419-81-5

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Basic information

Product Name: 9-phenylsulfonyl-2-(1-phenylsulfonyl-2-methyl-1H-indol-3-yl)-3-nitro-9H-carbazole
Synonyms:
CAS NO:1401419-81-5
Molecular Formula:
Molecular Weight: 621.694
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: 9-phenylsulfonyl-2-(1-phenylsulfonyl-2-methyl-1H-indol-3-yl)-3-nitro-9H-carbazole(CAS DataBase Reference)
NIST Chemistry Reference: 9-phenylsulfonyl-2-(1-phenylsulfonyl-2-methyl-1H-indol-3-yl)-3-nitro-9H-carbazole(1401419-81-5)
EPA Substance Registry System: 9-phenylsulfonyl-2-(1-phenylsulfonyl-2-methyl-1H-indol-3-yl)-3-nitro-9H-carbazole(1401419-81-5)

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: 1401419-81-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401419-81-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,4,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1401419-81:
(9*1)+(8*4)+(7*0)+(6*1)+(5*4)+(4*1)+(3*9)+(2*8)+(1*1)=115
115 % 10 = 5
So 1401419-81-5 is a valid CAS Registry Number.

1401419-81-5Upstream product

4637-24-5 N,N-dimethyl-formamide dimethyl acetal

1401419-81-5Downstream Products

1401419-81-5Relevant academic research and scientific papers

An improved synthesis of carbazoles via domino reaction of N-protected-2-methylindoles with DMF-DMA/DMA-DMA

Sureshbabu, Radhakrishnan,Mohanakrishnan, Arasambattu K.

, p. 913 - 918 (2012)

An efficient synthesis of carbazole analogs has been achieved via interaction of N-protected-2-methylindoles with N,N-dimethylformamide dimethylacetal as well as N,N-dimethylacetamide dimethylacetal in the presence of pyrrolidine or 1,4-diazabicyclo(2.2.2

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