32767-70-7

Basic information

• Product Name: 2H-Pyran, tetrahydro-2-(pentyloxy)-
• CAS NO: 32767-70-7
• Molecular Formula: C10H20O2
• Molecular Weight: 172.268
• Mol File: 32767-70-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2H-Pyran, tetrahydro-2-(pentyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran, tetrahydro-2-(pentyloxy)-(32767-70-7)
• EPA Substance Registry System: 2H-Pyran, tetrahydro-2-(pentyloxy)-(32767-70-7)

Safety Data

• Hazardous Substances Data: 32767-70-7(Hazardous Substances Data)

Upstream product

• 159598-02-4 5-Pentyloxy-5-phenylsulfanyl-pentan-1-ol 
• 2859-78-1 4-Bromoveratrole 
• 71233-40-4 5-(tetrahydro-2H-pyran-2-yloxy)pentylmagnesium bromide 
• 110-87-2 3,4-dihydro-2H-pyran 

Downstream Products

• 6581-66-4 2-methoxytetrahydropyran 
• 71-41-0 pentan-1-ol 
• 628-63-7 1-pentyl acetate 
• 67217-57-6 2-(2-methallyl)tetrahydro-2H-pyran 
• 1253279-28-5 C₁₆H₃₀O₃ 
• 167824-65-9 3-[(4R,5S,6S,7R)-4,7-Dibenzyl-5,6-dihydroxy-3-(5-hydroxy-pentyl)-2-oxo-[1,3]diazepan-1-ylmethyl]-benzoic acid ethyl ester 
• 167824-48-8 (4R,5S,6S,7R)-4,7-Dibenzyl-5,6-dihydroxy-1-(5-hydroxy-pentyl)-3-naphthalen-2-ylmethyl-[1,3]diazepan-2-one 
• 167824-71-7 (4R,5S,6S,7R)-4,7-Dibenzyl-5,6-dihydroxy-1-(3-hydroxymethyl-benzyl)-3-(5-hydroxy-pentyl)-[1,3]diazepan-2-one 
• 167824-58-0 (4R,5S,6S,7R)-4,7-Dibenzyl-5,6-dihydroxy-1-(3-hydroxy-benzyl)-3-(5-hydroxy-pentyl)-[1,3]diazepan-2-one 
• 167824-51-3 (4R,5S,6S,7R)-4,7-Dibenzyl-5,6-dihydroxy-1-(4-hydroxymethyl-benzyl)-3-(5-hydroxy-pentyl)-[1,3]diazepan-2-one 
• 167824-49-9 (4R,5S,6S,7R)-1,4,7-Tribenzyl-5,6-dihydroxy-3-(5-hydroxy-pentyl)-[1,3]diazepan-2-one 
• 167824-61-5 (4R,5S,6S,7R)-4,7-Dibenzyl-1-cyclopropylmethyl-5,6-dihydroxy-3-(5-hydroxy-pentyl)-[1,3]diazepan-2-one 
• 20965-36-0 2-(phenylthio)tetrahydro-2H-pyran 
• 110-62-3 pentanal 

Relevant articles and documents

Unprecedented polymer-supported π-acid: Synthesis and its application as a promoter to the monothioacetalization of acetals

A novel polymer was synthesized by copolymerization of styrene monomer bearing dicyanoketene acetal functionality and ethylene glycol dimethacrylate, and used successfully as a recyclable π-acid catalyst in monothioacetalization of aromatic, aliphatic, acyclic, and cyclic acetals with thiophenol and phenylthiotrimethylsilane.

Stereoselective synthesis of alkenyl alcohols using dissolving metal(Ca,Na) reduction

Use of the calcium-ethylenediamine and sodium-liquid ammonia reduction systems for the ring opening of dihydropyran derivatives was studied. (Z)-Alkenyl alcohols and (E)-alkenyl alcohols were stereoselectively synthesized respectively.