4-ACETAMIDOBENZONITRILE

  • Name: 4-ACETAMIDOBENZONITRILE
  • CAS: 35704-19-9
  • Purity: 99%
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Manufacturer Supply Best Quality 4-ACETAMIDOBENZONITRILE 35704-19-9 with Efficient Transportation

  • Molecular Formula: C9H8N2O
  • Molecular Weight: 160.175
  • Appearance/Colour: off-white crystalline powder and chunks 
  • Vapor Pressure: 2.34E-06mmHg at 25°C 
  • Melting Point: 206-208 °C(lit.) 
  • Refractive Index: 1.557 
  • Boiling Point: 392.1 °C at 760 mmHg 
  • PKA: 14.09±0.70(Predicted) 
  • Flash Point: 191 °C 
  • PSA： 52.89000 
  • Density: 1.16 g/cm3  
  • LogP: 1.58968 

4-ACETAMIDOBENZONITRILE(Cas 35704-19-9) Usage

InChI:InChI=1/C9H8N2O/c1-7(12)11-9-4-2-8(6-10)3-5-9/h2-5H,1H3,(H,11,12)

35704-19-9 Relevant articles

Design and synthesis of 3,5-substituted 1,2,4-oxadiazoles as catalytic inhibitors of human DNA topoisomerase IIα

Dolenc, Marija Sollner,Loboda, Kaja Bergant,Perdih, Andrej,Valjavec, Katja,Wolber, Gerhard,?tampar, Martina,?egura, Bojana,Filipi?, Metka

, (2020)

Cancer constitutes a group of diseases l...

Amine-Linked Covalent Organic Frameworks as a Platform for Postsynthetic Structure Interconversion and Pore-Wall Modification

Grunenberg, Lars,Savasci, G?kcen,Terban, Maxwell W.,Duppel, Viola,Moudrakovski, Igor,Etter, Martin,Dinnebier, Robert E.,Ochsenfeld, Christian,Lotsch, Bettina V.

supporting information, p. 3430 - 3438 (2021/04/07)

Covalent organic frameworks have emerged...

Preparation method of green visible light catalyzed acetamide compound

-

Paragraph 0030-0031, (2021/12/02)

The invention discloses a preparation me...

Ethyl 2-Cyano-2-(2-nitrobenzenesulfonyloxyimino) Acetate (ortho-NosylOXY)-Mediated Double Beckmann Rearrangement of Ketoximes under Microwave Irradiation: A Mechanistic Perception

Dev, Dharm,Kalita, Tapasi,Mondal, Tanmay,Mandal, Bhubaneswar

, p. 1427 - 1435 (2021/01/04)

A method for Beckmann rearrangement usin...

A Molecular Iron-Based System for Divergent Bond Activation: Controlling the Reactivity of Aldehydes

Chatterjee, Basujit,Jena, Soumyashree,Chugh, Vishal,Weyhermüller, Thomas,Werlé, Christophe

, p. 7176 - 7185 (2021/06/30)

The direct synthesis of amides and nitri...

35704-19-9 Process route

N-(4-Cyano-phenyl)-N'-(4-nitro-phenyl)-acetamidine
128915-29-7

N-(4-Cyano-phenyl)-N'-(4-nitro-phenyl)-acetamidine

4-nitro-aniline
100-01-6,104810-17-5

4-nitro-aniline

N-(4-cyanophenyl)acetamide
35704-19-9

N-(4-cyanophenyl)acetamide

Conditions
Conditions Yield
With hydrogenchloride; In 1,4-dioxane; water; at 40 ℃; Rate constant;
N-(4-(2-phenylethynyl)phenyl)acetamide

N-(4-(2-phenylethynyl)phenyl)acetamide

benzonitrile
100-47-0

benzonitrile

N-(4-cyanophenyl)acetamide
35704-19-9

N-(4-cyanophenyl)acetamide

Conditions
Conditions Yield
With N-iodo-succinimide; trimethylsilylazide; In 1,2-dichloro-ethane; acetonitrile; at 20 - 70 ℃; for 7h;
66%
50 %Chromat.

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