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2-(4-methoxyphenyl)-1-oxoisoindoline-5-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19048-31-8 Structure
  • Basic information

    1. Product Name: 2-(4-methoxyphenyl)-1-oxoisoindoline-5-carbonitrile
    2. Synonyms: 2-(4-methoxyphenyl)-1-oxoisoindoline-5-carbonitrile
    3. CAS NO:19048-31-8
    4. Molecular Formula:
    5. Molecular Weight: 264.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19048-31-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-methoxyphenyl)-1-oxoisoindoline-5-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-methoxyphenyl)-1-oxoisoindoline-5-carbonitrile(19048-31-8)
    11. EPA Substance Registry System: 2-(4-methoxyphenyl)-1-oxoisoindoline-5-carbonitrile(19048-31-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 19048-31-8(Hazardous Substances Data)

19048-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19048-31-8 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 19048-31:
(7*1)+(6*9)+(5*0)+(4*4)+(3*8)+(2*3)+(1*1)=108
108 % 10 = 8
So 19048-31-8 is a valid CAS Registry Number.

19048-31-8Upstream product

19048-31-8Downstream Products

19048-31-8Relevant articles and documents

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)

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.

Hantzsch ester triggered metal-free cascade approach to isoindolinones

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

supporting information, p. 1866 - 1870 (2018/04/14)

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.

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