931-97-5

  • Product Name:Cyclohexanone cyanohydrin
  • Molecular Formula:C7H11 N O
  • Purity:99%
  • Molecular Weight:125.17
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Product Details

Quality Factory Supply Best Quality Cyclohexanone cyanohydrin 931-97-5 with Efficient Delivery

  • Molecular Formula:C7H11 N O
  • Molecular Weight:125.17
  • Appearance/Colour:Colourless solid. Typical sharp nitrile odor 
  • Vapor Pressure:0.0113mmHg at 25°C 
  • Melting Point:32-35ºC 
  • Refractive Index:1.4693 
  • Boiling Point:232.1 °C at 760 mmHg 
  • PKA:11.45±0.20(Predicted) 
  • Flash Point:112.1 °C 
  • PSA:44.02000 
  • Density:1.06 g/cm3 
  • LogP:1.20518 

1-HYDROXY-1-CYCLOHEXANECARBONITRILE(Cas 931-97-5) Usage

Description

Cyclohexanone cyanohydrin is a brown solid.
Uses Cyclohexanone cyanohydrin was employed as substrate during high-throughput screening assay for hydroxynitrile lyase activity. It was used in preparation of 1-aminomethyl cyclohexanol via catalytic hydrogenation reaction.

InChI:InChI=1/C7H11NO/c8-6-7(9)4-2-1-3-5-7/h9H,1-5H2

931-97-5 Relevant articles

CO2-Enabled Cyanohydrin Synthesis and Facile Iterative Homologation Reactions**

Juhl, Martin,Petersen, Allan R.,Lee, Ji-Woong

supporting information, p. 228 - 232 (2020/11/30)

Thermodynamic and kinetic control of a c...

Radical-mediated aerobic oxidation of substituted styrenes and stilbenes

Aman, Hasil,Chiu, Wei-Hua,Chuang, Gary Jing,Liu, Pin-Heng

, p. 20103 - 20106 (2021/12/02)

A 2,2-azobis(isobutyronitrile)-catalyzed...

Production process of high-purity and high-yield spirodiclofen

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Paragraph 0046; 0051; 0067, (2019/03/08)

The invention relates to the technical f...

SPIRO-OXAZOLONES

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Page/Page column 75, (2015/09/28)

The present invention provides spiro-oxa...

931-97-5 Process route

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

2-hydroxy-2-methylpropanenitrile
75-86-5

2-hydroxy-2-methylpropanenitrile

1-hydroxy-1-cyclohexanecarbonitrile
931-97-5

1-hydroxy-1-cyclohexanecarbonitrile

Conditions
Conditions Yield
With Hevea brasiliensis (S)-hydroxynitrile lyase; pH=4.5; aq. buffer; Enzymatic reaction;
100%
With titanium(IV) isopropylate; dl-3-(2-hydroxy-1-naphthylidene)-imino-ε-caprolactam (Nap-ACL); In dichloromethane; for 3h; Ambient temperature;
99%
With ytterbium(III) isopropoxide; In tetrahydrofuran; for 0.5h; Ambient temperature;
94%
With lanthanum(III) isopropoxide; In tetrahydrofuran; at 20 ℃;
81%
With sodium hydroxide; In di-isopropyl ether; at 20 ℃; for 6h;
68%
With potassium carbonate;
 
hydrogen cyanide
74-90-8

hydrogen cyanide

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

1-hydroxy-1-cyclohexanecarbonitrile
931-97-5

1-hydroxy-1-cyclohexanecarbonitrile

Conditions
Conditions Yield
in Gegenwart von Kaliumcarbonat,-hydroxyd oder -cyanid;
 
 
 
With basic ion exchanger;
 
With potassium hydroxide;
 
With citrate-phosphate buffer; Arabidopsis thaliana hydroxynitrile lyase; In di-isopropyl ether; at 10 ℃; for 3h; pH=5.0;
 

931-97-5 Upstream products

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    hydrogen cyanide

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931-97-5 Downstream products

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    ethyl 2-cyano-2-(1-cyanocyclohexyl)acetate

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    hydrogen cyanide

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    108-94-1

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