4295-99-2

Basic information

• Product Name: 4-Cyanotetrahydro-4H-pyran
• Synonyms: 4-CYANOTETRAHYDRO-4H-PYRAN;4-Cyanotetrahydropyran;tetrahydro-2H-pyran-4-carbonitrile(SALTDATA: FREE);Tetrahydro-pyran-4-carbonitrile;oxane-4-carbonitrile;2H-Pyran-4-carbonitrile, tetrahydro-;4-cyanotetrahydropiran
• CAS NO: 4295-99-2
• Molecular Formula: C₆H₉NO
• Molecular Weight: 111.14
• Mol File: 4295-99-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 224.027 °C at 760 mmHg
• Flash Point: 92.165 °C
• Appearance: /
• Density: 1.012 g/cm³
• Vapor Pressure: 0.0932mmHg at 25°C
• Refractive Index: 1.448
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-Cyanotetrahydro-4H-pyran(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Cyanotetrahydro-4H-pyran(4295-99-2)
• EPA Substance Registry System: 4-Cyanotetrahydro-4H-pyran(4295-99-2)

Safety Data

• RIDADR: UN2811
• HazardClass: IRRITANT
• Hazardous Substances Data: 4295-99-2(Hazardous Substances Data)

Usage

Uses

Tetrahydro-2H-Pyran-4-Carbonitrile is used in preparation of substituted Amide compounds as farnesoid X receptor modulators.

InChI:InChI=1/C6H9NO/c7-5-6-1-3-8-4-2-6/h6H,1-4H2

Upstream product

• 50675-18-8 3,4,5,6-tetrahydro-2H-pyran-4-carbaldehyde 

Downstream Products

• 137052-08-5 1-(tetrahydro-2H-pyran-4-yl)ethan-1-one 
• 7403-84-1 1-tetrahydropyran-4-yl-butan-1-one semicarbazone 
• 7502-01-4 4-methyl-1-tetrahydropyran-4-yl-pentan-1-one semicarbazone 
• 7403-99-8 1-tetrahydropyran-4-yl-heptan-1-one semicarbazone 
• 92325-74-1 1-tetrahydropyran-4-yl-propan-1-one-(2,4-dinitro-phenylhydrazone) 
• 93046-48-1 1-tetrahydropyran-4-yl-pentan-1-one-(2,4-dinitro-phenylhydrazone) 
• 96978-43-7 1-tetrahydropyran-4-yl-hexan-1-one-(2,4-dinitro-phenylhydrazone) 
• 1350894-89-1 C₂₀H₂₁N₃O 
• 1092544-98-3 N-(4-fluoro-2-(methylsulfonyl)benzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-2H-pyran-4-yl)-1,6-dihydropyrimidine-4-carboxamide 
• 1092544-99-4 N-(2-(N,N-dimethylsulfamoyl)-4-fluorobenzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-2H-pyran-4-yl)-1,6-dihydropyrimidine-4-carboxamide 
• 1092545-00-0 N-(4-fluoro-2-(1,1-dioxo-1λ6-[1,2]thiazinan-2-yl)benzylcarbamoyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-2H-pyran-4-yl)-1,6-dihydropyrimidine-4-carboxamide 
• 1092544-94-9 N-(4-fluoro-2-(1H-1,2,4-triazol-1-yl)benzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-2H-pyran-4-yl)-1,6-dihydropyrimidine-4-carboxamide 
• 1092544-95-0 N-(4-fluoro-2-(5-methyl-1H-1,2,4-triazol-1-yl)benzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-2H-pyran-4-yl)-1,6-dihydropyrimidine-4-carboxamide 
• 1092544-96-1 N-(4-fluoro-2-(5-methyl-1H-1,2,3-triazol-1-yl)benzyl)-5-hydroxy-1-methyl-6-oxo-2-(tetrahydro-2H-pyran-4-yl)-1,6-dihydropyrimidine-4-carboxamide 

Relevant articles and documents

An efficient catalytic method for the Beckmann rearrangement of ketoximes to amides and aldoximes to nitriles mediated by propylphosphonic anhydride (T3P)

An efficient method for the Beckmann rearrangement of ketoximes to amides mediated by a catalytic amount (15 mol %) of propylphosphonic anhydride (T3P) is described. Aldoximes underwent second order Beckmann rearrangement to provide the corresponding nitriles in excellent yields on reacting with T3P (15 mol %) at room temperature. The main advantages of this environmentally friendly protocol include procedural simplicity, and particularly ease of isolation of the products.