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1-oxo-2-phenylisoindoline-5-carbonitrile is a chemical compound with the molecular formula C15H8N2O. It is a derivative of isoindoline, a heterocyclic organic compound containing a nitrogen atom in a six-membered aromatic ring. The compound features a carbonitrile group (-CN) at the 5-position, a phenyl group (C6H5) at the 2-position, and a carbonyl group (C=O) at the 1-position. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is typically synthesized through various chemical reactions, such as condensation or cyclization, and can be further functionalized to create a range of derivatives with diverse properties and applications.

19048-30-7

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19048-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19048-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,4 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19048-30:
(7*1)+(6*9)+(5*0)+(4*4)+(3*8)+(2*3)+(1*0)=107
107 % 10 = 7
So 19048-30-7 is a valid CAS Registry Number.

19048-30-7Downstream Products

19048-30-7Relevant academic research and scientific papers

Hantzsch ester triggered metal-free cascade approach to isoindolinones

Tian, Youping,Wei, Junmei,Wang, Meng,Li, Gaoqiang,Xu, Feng

, p. 1866 - 1870 (2018)

Disclosed herein is an expedient synthesis of biologically important isoindolinone derivatives from reactions of 2-formylbenzoic acids with various amines. This method operates via a deliberately designed catalyst-free tandem reductive amination/cyclization cascade event triggered by a transfer hydrogenation process with easily available Hantzsch ester as the organic hydride source. The ease of operation, mild reaction conditions, facile accessibility of the starting materials, and easy scalability of the current method distinguish it from the other precedent protocols, thus enable it a practical approach to the syntheses of valuable isoindolinone-incorporated drugs.

A facile and efficient method for the synthesis of N-substituted isoindolin-1-one derivatives under Pd(OAc)2/HCOOH system

Zhou, Yang,Chen, Ping,Lv, Xue,Niu, Junxing,Wang, Yingying,Lei, Min,Hu, Lihong

, p. 2232 - 2235 (2017/05/16)

A facile and efficient method for the synthesis of N-substituted isoindolin-1-one derivatives from 2-formylbenzoic acid and amine under Pd(OAc)2/HCOOH system has been described. The whole process is carried out in ligand-free conditions and furnished the desired products by reductive intramolecular cyclization. Furthermore, this procedure is applied successfully for the modification of natural products, such as vindoline and estrone.

HETEROCYCLIC COMPOUND

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, (2017/02/09)

The present invention provide a heterocyclic compound having a HDAC inhibitory action, and useful for the treatment of autoimmune diseases and/or inflammatory diseases, graft versus host disease, cancers, central nervous diseases including neurodegenerative diseases, Charcot-Marie-Tooth disease and the like, and a pharmaceutical composition comprising the compound. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.

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