Cas 420783-79-5,2,3-dihydro-1-(N,N-dimethylsulfamoyl)-4-trimethylsilyl-1H-indole-5-(N-phenyl)carboxamide

420783-79-5

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Basic information

Product Name: 2,3-dihydro-1-(N,N-dimethylsulfamoyl)-4-trimethylsilyl-1H-indole-5-(N-phenyl)carboxamide
Synonyms: 2,3-dihydro-1-(N,N-dimethylsulfamoyl)-4-trimethylsilyl-1H-indole-5-(N-phenyl)carboxamide
CAS NO:420783-79-5
Molecular Formula:
Molecular Weight: 417.604
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: 2,3-dihydro-1-(N,N-dimethylsulfamoyl)-4-trimethylsilyl-1H-indole-5-(N-phenyl)carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 2,3-dihydro-1-(N,N-dimethylsulfamoyl)-4-trimethylsilyl-1H-indole-5-(N-phenyl)carboxamide(420783-79-5)
EPA Substance Registry System: 2,3-dihydro-1-(N,N-dimethylsulfamoyl)-4-trimethylsilyl-1H-indole-5-(N-phenyl)carboxamide(420783-79-5)

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: 420783-79-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 420783-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,0,7,8 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 420783-79:
(8*4)+(7*2)+(6*0)+(5*7)+(4*8)+(3*3)+(2*7)+(1*9)=145
145 % 10 = 5
So 420783-79-5 is a valid CAS Registry Number.

420783-79-5Upstream product

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420783-79-5Relevant academic research and scientific papers

Regioselective ortho-directed metalation and electrophilic substitution of indole- and indoline-5-(N-phenyl)carboxamides

Rousseau, Jean-Fran?ois,Dodd, Robert H.

, p. 2289 - 2304 (2007/10/03)

Treatment of 1-(N,N-dimethylsulfamoyl)-1H-indole-5-(N-phenyl) carboxamide (1) with s-butyllithium at -80°C in THF followed by addition of an electrophile gave exclusively the product of C-2 substitution. A second metalation-substitution cycle on this prod

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