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N-(2-cyanophenyl)cyclohexanecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220383-49-3 Structure
  • Basic information

    1. Product Name: N-(2-cyanophenyl)cyclohexanecarboxamide
    2. Synonyms: N-(2-cyanophenyl)cyclohexanecarboxamide
    3. CAS NO:220383-49-3
    4. Molecular Formula: C14H16N2O
    5. Molecular Weight: 228.28964
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220383-49-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-cyanophenyl)cyclohexanecarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-cyanophenyl)cyclohexanecarboxamide(220383-49-3)
    11. EPA Substance Registry System: N-(2-cyanophenyl)cyclohexanecarboxamide(220383-49-3)
  • 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: 220383-49-3(Hazardous Substances Data)

220383-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220383-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,8 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220383-49:
(8*2)+(7*2)+(6*0)+(5*3)+(4*8)+(3*3)+(2*4)+(1*9)=103
103 % 10 = 3
So 220383-49-3 is a valid CAS Registry Number.

220383-49-3Relevant articles and documents

A combinatorial approach towards 2-acyl-3-amino-indole derivatives

Nettekoven

, p. 8251 - 8254 (2000)

A widely applicable reaction sequence towards functionalised 2-acyl-3-amino-indole derivatives is presented. A set of 205 indole derivatives were prepared, in a solution phase combinatorial fashion, by coupling a reliable reaction protocol to a rapid puri

Pd-Catalyzed tandem reaction of N-(2-cyanoaryl)benzamides with arylboronic acids: synthesis of quinazolines

Zhu, Jianghe,Shao, Yinlin,Hu, Kun,Qi, Linjun,Cheng, Tianxing,Chen, Jiuxi

supporting information, p. 8596 - 8603 (2018/11/27)

The synthesis of 2,4-disubstituted quinazolines by a palladium-catalyzed reaction of arylboronic acids with N-(2-cyanoaryl)benzamides has been developed with moderate to excellent yields. The method shows good functional group tolerance. In particular, ha

Copper-catalyzed oxidative ring closure of ortho-cyanoanilides with hypervalent iodonium salts: Arylation-ring closure approach to iminobenzoxazines

Aradi, Klra,Novk, Zoltn

supporting information, p. 371 - 376 (2015/03/05)

A novel, highly modular synthetic methodology with high functional group tolerance was developed for the construction of iminobenzoxazine derivatives from ortho-cyanoanilides and diaryliodonium triflates via an oxidative arylation-cyclization path. The reaction is supposed to involve the formation of highly active aryl-copper(III) species. In this novel transformation, copper(II) triflate was used as catalyst in 1,2-dichloroethane or ethyl acetate and the reaction takes place at 75 °C in 2-16 h.

1-(N-PHENYLAMINOALKYL)-PIPERAZINE DERIVATIVES SUBSTITUTED AT POSITION 2 OF THE PHENYL RING

-

Page 17-18, (2008/06/13)

Disclosed herein are novel compounds and methods for the treatment of disorders of the lower urinary tract. The novel compounds are aniline derivatives substituted at position 2 of the aniline ring. The methods comprise the administration of the novel com

1-(N-phenylaminoalkyl)piperazine derivatives substituted at position 2 of the phenyl ring

-

, (2008/06/13)

The present invention is directed to novel 1-(N-phenylaminoalkyl)piperazine derivatives substituted at the position 2 of the phenyl ring. Pharmaceutical compositions comprising the compounds of the invention also are contemplated. The compounds of the pre

1-(N-phenylaminoalkyl)piperazine derivatives substituted at position 2 of the phenyl ring

-

, (2008/06/13)

Disclosed herein are novel compounds and methods for the treatment of disorders of the lower urinary tract. The novel compounds are aniline derivatives substituted at position 2 of the aniline ring. The methods comprise the administration of the novel com

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