107833-76-1

Basic information

• Product Name: 3-NITROPROPYL 2-TETRAHYDROPYRANYL ETHER
• Synonyms: 2-(3-NITROPROPOXY)TETRAHYDROPYRANE;3-NITROPROPYL 2-TETRAHYDROPYRANYL ETHER;3-NITROPROPYL-2-TETRAHYDROPYRANYL ETHER APPOX. 93%
• CAS NO: 107833-76-1
• Molecular Formula: C₈H₁₅NO₄
• Molecular Weight: 189.21
• Mol File: 107833-76-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-NITROPROPYL 2-TETRAHYDROPYRANYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITROPROPYL 2-TETRAHYDROPYRANYL ETHER(107833-76-1)
• EPA Substance Registry System: 3-NITROPROPYL 2-TETRAHYDROPYRANYL ETHER(107833-76-1)

Safety Data

• Hazardous Substances Data: 107833-76-1(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 25182-84-7 3-nitropropan-1-ol 
• 33821-94-2 3-(tetrahydro-2H-pyran-2-yloxy)propyl bromide 

Downstream Products

• 94371-25-2 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-4,5-dihydro-isoxazole 
• 94371-26-3 5-[(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-cyclohexylmethyl]-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazole 
• 910109-62-5 5-iodo-6-methyl-2-oxo-1-(3-trifluoromethyl-phenyl)-1,2-dihydro-pyridine-3-carboxylic acid {3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-isoxazol-5-ylmethyl}-amide 

Relevant articles and documents

Catalytic Asymmetric Synthesis of Isoxazolines from Silyl Nitronates

1,3-Dipolar cycloadditions of triisopropylsilyl nitronates and 2-alkylacroleins produced isoxazolines bearing a chiral quaternary center in high yields and enantioselectivities with the aid of a chiral oxazaborolidine catalyst. One chiral isoxazoline product was converted to (R)-(+)-Tanikolide in 9 steps in a total yield of 43%. (Chemical Equation Presented).

3-Nitropropanal and 3-Nitropropanol: Preparation of the Parent Compounds and Derivatives

3-Nitropropanal has been prepared for the first time by 1,4-nitrite addition to acrolein.Several acetals of 3-nitropropanal are described, as well as 3-nitropropanol and some of its ethers. 3-Nitropropanol has been obtained by borane-dimethyl sulfide reduction of both 3-nitropropanal and 3-nitropropanoic acid.These reactions make available a variety of nitro compounds known as, or expected to become, highly useful and versatile building blocks for organic syntheses.