Main product

52688-11-6

  • Product Name：Cyclohexyl cyanoacetate
  • Molecular Formula：C9H13NO2
  • Specifications：99%
  • Molecular Weight：167.208
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Product Details;

CasNo： 52688-11-6

Molecular Formula： C9H13NO2

Cost-effective customized wholesale Cyclohexyl cyanoacetate 52688-11-6

  • Molecular Formula:C9H13NO2
  • Molecular Weight:167.208
  • Vapor Pressure:0.0028mmHg at 25°C 
  • Refractive Index:1.4620 (589.3 nm 20℃) 
  • Boiling Point:285.4 °C at 760 mmHg 
  • Flash Point:130.3 °C 
  • PSA：50.09000 
  • Density:1.06 g/cm3 
  • LogP:1.77598 

Cyclohexyl cyanoacetate(Cas 52688-11-6) Usage

General Description

Cyclohexyl cyanoacetate is a chemical compound with the molecular formula C10H15NO2. It is a colorless liquid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Cyclohexyl cyanoacetate is known for its strong cyano group, which makes it a versatile building block in organic synthesis. It is used as a precursor in the production of various compounds, including insecticides, herbicides, and pharmaceutical drugs. Additionally, it is also used as a solvent in some industrial processes. Overall, cyclohexyl cyanoacetate plays a crucial role in the development of various chemical products and has a wide range of applications in the pharmaceutical and agricultural industries.

InChI:InChI=1/C9H13NO2/c10-7-6-9(11)12-8-4-2-1-3-5-8/h8H,1-6H2

52688-11-6 Relevant articles

Development of the First Two-Pore Domain Potassium Channel TWIK-Related K+ Channel 1-Selective Agonist Possessing in Vivo Antinociceptive Activity

Vivier, Delphine,Soussia, Ismail Ben,Rodrigues, Nuno,Lolignier, Stéphane,Devilliers, Ma?ly,Chatelain, Franck C.,Prival, Laetitia,Chapuy, Eric,Bourdier, Geoffrey,Bennis, Khalil,Lesage, Florian,Eschalier, Alain,Busserolles, Jér?me,Ducki, Sylvie

supporting information, p. 1076 - 1088 (2017/02/19)

The TWIK-related K+ channel, TREK-1, has...

Thiophene inhibitors of PDE4: Crystal structures show a second binding mode at the catalytic domain of PDE4D2

Nankervis, Jacob L.,Feil, Susanne C.,Hancock, Nancy C.,Zheng, Zhaohua,Ng, Hooi-Ling,Morton, Craig J.,Holien, Jessica K.,Ho, Patricia W.M.,Frazzetto, Mark M.,Jennings, Ian G.,Manallack, David T.,John Martin,Thompson, Philip E.,Parker, Michael W.

supporting information; experimental part, p. 7089 - 7093 (2012/01/06)

PDE4 inhibitors have been identified as ...

A new class of small molecule RNA polymerase inhibitors with activity against Rifampicin-resistant Staphylococcus aureus1

Arhin, Francis,Belanger, Odette,Ciblat, Stephane,Dehbi, Mohammed,Delorme, Daniel,Dietrich, Evelyne,Dixit, Dilip,Lafontaine, Yanick,Lehoux, Dario,Liu, Jing,McKay, Geoffrey A.,Moeck, Greg,Reddy, Ranga,Rose, Yannick,Srikumar, Ramakrishnan,Tanaka, Kelly S.E.,Williams, Daniel M.,Gros, Philippe,Pelletier, Jerry,Parr Jr., Thomas R.,Far, Adel Rafai

, p. 5812 - 5832 (2007/10/03)

The RNA polymerase holoenzyme is a prove...

52688-11-6 Process route

cyanoacetic acid
372-09-8

cyanoacetic acid

cyclohexanol
108-93-0

cyclohexanol

cyclohexyl 2-cyanoacetate
52688-11-6

cyclohexyl 2-cyanoacetate

Conditions
Conditions Yield
With sulfuric acid; In benzene; for 2.5h; Heating;
100%
With sulfuric acid; In chloroform; for 5h; Reflux;
78%
With sulfuric acid; In toluene; for 24h; Reflux;
77%
With hydrocarbon; toluene-4-sulfonic acid; unter Entfernung des entstehenden Wassers durch azeotrope Destillation;
cyclohexyl 2-cyanoacetate
52688-11-6

cyclohexyl 2-cyanoacetate

Conditions
Conditions Yield
/BRN= 863882/, HCN;

52688-11-6 Upstream products

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  • 108-93-0
    108-93-0

    cyclohexanol

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