Cas 1198565-08-0,N-(4-fluorophenyl)-1H-indole-1-carboxamide

1198565-08-0

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Basic information

Product Name: N-(4-fluorophenyl)-1H-indole-1-carboxamide
Synonyms: N-(4-fluorophenyl)-1H-indole-1-carboxamide
CAS NO:1198565-08-0
Molecular Formula:
Molecular Weight: 254.264
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: N-(4-fluorophenyl)-1H-indole-1-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-fluorophenyl)-1H-indole-1-carboxamide(1198565-08-0)
EPA Substance Registry System: N-(4-fluorophenyl)-1H-indole-1-carboxamide(1198565-08-0)

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: 1198565-08-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198565-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,5,6 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1198565-08:
(9*1)+(8*1)+(7*9)+(6*8)+(5*5)+(4*6)+(3*5)+(2*0)+(1*8)=200
200 % 10 = 0
So 1198565-08-0 is a valid CAS Registry Number.

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1198565-08-0Relevant academic research and scientific papers

Copper(I)-Catalyzed N-Carboxamidation of Indoles with Isocyanates: Facile and General Method for the Synthesis of Indole-1-carboxamides

Chen, Jinyang,Hu, Li,Wang, Haiying,Liu, Lingrong,Yuan, Binfang

, p. 3949 - 3954 (2019/06/24)

A facile and general method for the synthesis of indole-1-carboxamides was developed via copper(I)-catalyzed N-carboxamidation of indoles with isocyanates under mild reaction conditions. This process is scalable and tolerates a wide spectrum of indoles and isocyanates to deliver corresponding products in good to excellent yields, providing a viable synthetic approach to indole-1-carboxamides, which can be used for the treatment of inflammatory diseases and diabetes.

AlMe3-mediated regio- and chemoselective reactions of indole with carbamoyl electrophiles

Velavan,Sumathi,Balasubramanian

, p. 3148 - 3157 (2013/06/27)

Herein, we report the regio- and chemoselective reactions of indole with carbamoyl electrophiles in presence of AlMe3. Indole-3-carboxamide was prepared in one-step from a reaction of indole with tertiary carbamoylimidazole in the presence AlMe

Gold-catalyzed intramolecular hydroamination of terminal alkynes in aqueous media: efficient and regioselective synthesis of indole-1-carboxamides

Ye, Deju,Wang, Jinfang,Zhang, Xu,Zhou, Yu,Ding, Xiao,Feng, Enguang,Sun, Haifeng,Liu, Guannan,Jiang, Hualiang,Liu, Hong

experimental part, p. 1201 - 1208 (2010/04/26)

Using [Au(PPh3)]Cl/Ag2CO3-catalyzed 5-endo-dig cyclization in water under microwave irradiation, we developed a fast and green route to prepare indole-1-carboxamides from N′-substituted N-(2-alkynylphenyl)ureas. The descri

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