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1H-Indole-5-carboxamide, N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

329185-67-3

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329185-67-3 Usage

Structure

An amide derivative of indole with a phenyl group attached to the nitrogen atom of the carboxamide group

Usage

Widely used in the pharmaceutical industry as an intermediate in the synthesis of various pharmaceutical drugs

Biological activity

The N-phenylsubstitution enhances the biological activity of the compound

Potential applications

As an antitumor agent, analgesic, anti-inflammatory, and inhibitor of protein kinase C

Promise

Showing promise as a potential candidate for the development of novel therapeutic agents

Check Digit Verification of cas no

The CAS Registry Mumber 329185-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,1,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 329185-67:
(8*3)+(7*2)+(6*9)+(5*1)+(4*8)+(3*5)+(2*6)+(1*7)=163
163 % 10 = 3
So 329185-67-3 is a valid CAS Registry Number.

329185-67-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-indole-5-(N-phenyl)carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Indole-5-carboxylic acid phenylamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:329185-67-3 SDS

329185-67-3Relevant academic research and scientific papers

Functionalization of indole at C-5 or C-7 via palladium-catalysed double carbonylation. A facile synthesis of indole ketocarboxamides and carboxamide dimers

Takács, Attila,Marosv?lgyi-Haskó, Diána,Kabak-Solt, Zsuzsanna,Damas, Liliana,Rodrigues, Fábio M.S.,Carrilho, Rui M.B.,Pineiro, Marta,Pereira, Mariette M.,Kollár, László

, p. 247 - 256 (2016)

Palladium-catalysed aminocarbonylation of 7-iodoindole derivatives (the parent compound and 5-bromo-7-iodoindole), as well as 5-iodoindole with various primary and secondary amines, including amino acid esters and chiral diamines, was carried out. In this

Aminocarbonylation of aryl iodides with primary and secondary amines in aqueous medium using polymer supported palladium-N-heterocyclic carbene complex as an efficient and heterogeneous recyclable catalyst

Qureshi, Ziyauddin S.,Revankar, Santosh A.,Khedkar, Mayur V.,Bhanage, Bhalchandra M.

, p. 148 - 153 (2015/02/20)

Aminocarbonylation of aryl iodides with primary and secondary aromatic/aliphatic amines to corresponding amides using polymer supported palladium-N-heterocyclic carbene complex (PS-Pd-NHC) as an efficient heterogeneous, recyclable catalyst is described. The catalytic system was optimized with respect to various reaction parameters to give excellent yield of desired products. The catalyst can be easily separated by simple filtration process and recycled further up to four consecutive recycle without loss in any activity and selectivity. The protocol is advantageous due to the ease in handling of the catalyst, simple workup procedure, and environmentally benign water as solvent and effective catalyst recyclability.

NOVEL RHO KINASE INHIBITORS AND METHODS OF USE

-

Page/Page column 87, (2012/10/18)

The subject invention concerns materials and methods for treating diseases and disorders associated with expression of Rho associated kinases (ROCKs). Examples of diseases and disorders contemplated within the scope of the invention include, but are not limited to, oncological disorders, cardiovascular diseases, CNS disorders, and inflammatory disorders. In one embodiment, a method of the invention comprises administering a therapeutically effective amount of one or more compounds of the present invention, or a composition comprising the compounds, to a person or animal in need of treatment. The subject invention also concerns compounds that inhibit ROCKs, and compositions that comprise the inhibitor compounds of the invention. Compounds contemplated within the scope of the invention include, but are not limited to, those compounds shown in Table (5).

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

Efficient electrochemical cleavage of N,N-dimethylaminosulfonyl-protected indoles

Largeron,Farrell,Rousseau,Fleury,Potier,Dodd

, p. 9403 - 9406 (2007/10/03)

Indoles protected at the N-1 position with the N,N-dimethylaminosulfonyl group were efficiently deprotected by electrolysis. Yields were in the 80-90% range and the method was compatible with a number of functional groups (nitrile, ester, chloride, carboxamide). (C) 2000 Elsevier Science Ltd.

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