Cas 1224969-96-3,2-butyl-N-phenyl-1H-indole-1-carboxamide

1224969-96-3

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Basic information

Product Name: 2-butyl-N-phenyl-1H-indole-1-carboxamide
Synonyms: 2-butyl-N-phenyl-1H-indole-1-carboxamide
CAS NO:1224969-96-3
Molecular Formula:
Molecular Weight: 292.381
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-butyl-N-phenyl-1H-indole-1-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-butyl-N-phenyl-1H-indole-1-carboxamide(1224969-96-3)
EPA Substance Registry System: 2-butyl-N-phenyl-1H-indole-1-carboxamide(1224969-96-3)

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: 1224969-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1224969-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,9,6 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1224969-96:
(9*1)+(8*2)+(7*2)+(6*4)+(5*9)+(4*6)+(3*9)+(2*9)+(1*6)=183
183 % 10 = 3
So 1224969-96-3 is a valid CAS Registry Number.

1224969-96-3Upstream product

1224969-96-3Downstream Products

1224969-96-3Relevant academic research and scientific papers

Silica-immobilized NHC-gold(I) complexes: Versatile catalysts for the functionalization of alkynes under batch and continuous flow conditions

Sarmiento, Jeymy T.,Suárez-Pantiga, Samuel,Olmos, Andrea,Varea, Teresa,Asensio, Gregorio

, p. 7146 - 7155 (2017)

Immobilized sterically demanding NHC-Au(I) complexes silica-[(IPrR)Au]Cl and silica-[(IAdPrR)Au]Cl are synthesized and characterized. These complexes are suitable catalysts in typical homogeneous Au(I)-catalyzed alkyne reactions such

Platinum-catalyzed, one-pot tandem synthesis of indoles and isoquinolines via sequential rearrangement of amides and aminocyclization

Okamoto, Noriko,Takeda, Kei,Yanada, Reiko

supporting information; experimental part, p. 7615 - 7625 (2011/02/25)

By using platinum(II) chloride as a Lewis acid catalyst, concise and efficient syntheses of indole carbamates, 1,2-dihydroisoquinoline carbamates, macrocyclic indole carbamates, indole ureas, and indole phosphoranes have been achieved via tandem Hofmann-t

NHC-stabilized gold(I) complexes: Suitable catalysts for 6-exo-dig heterocyclization of 1-(o-Ethynylaryl)ureas

Gimeno, Ana,Medio-Simon, Mercedes,De Arellano, Carmen Ramirez,Asensio, Gregorio,Cuenca, Ana B.

supporting information; scheme or table, p. 1900 - 1903 (2010/06/21)

Figure presented 3-substituted 1-(o-ethynylaryl)ureas 1 selectively undergo either 6-exo-dig or 5-endo-dig cyclization (to give 4-methylene-3,4-quinazolin- 2-ones 2 or indoles 3, respectively) depending on the choice of the metal, ligand, and reaction conditions. The best results (up to 96% yield) in the preparation of the hydroamination products 2 are achieved with the highly bulky NHC-stabilized cationic gold(I) complex [Au(IPr)]+. Conversely, ureas bearing an internal alkyne lead to the 5-endo-dig cyclization mode regardless of the gold(I) complex employed. Whereas the nature of the substituent at N-3 does not have any influence on the regiochemistry observed, it does, in some cases, affect the efficiency of these transformations.

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