180259-48-7

Basic information

• Product Name: 1-methoxy-4-((pent-4-en-1-yloxy)methyl)benzene
• Synonyms: 1-methoxy-4-((pent-4-en-1-yloxy)methyl)benzene
• CAS NO: 180259-48-7
• Molecular Weight: 206.285
• Mol File: 180259-48-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-methoxy-4-((pent-4-en-1-yloxy)methyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-((pent-4-en-1-yloxy)methyl)benzene(180259-48-7)
• EPA Substance Registry System: 1-methoxy-4-((pent-4-en-1-yloxy)methyl)benzene(180259-48-7)

Safety Data

• Hazardous Substances Data: 180259-48-7(Hazardous Substances Data)

Upstream product

• 821-09-0 n-Pent-4-enyl alcohol 
• 824-94-2 p-methoxybenzyl chloride 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 2746-25-0 p-Methoxybenzyl bromide 
• 923571-35-1 1-Methoxy-4-(5-phenylsulfanyl-pentyloxymethyl)-benzene 
• 74203-20-6 5-benzoyloxy-1-iodopentane 
• 57774-95-5 5-(phenylthio)-1-pentanol 
• 55162-82-8 1-benzoyloxypentan-5-ol 
• 111-29-5 1 ,5-pentanediol 
• 923571-34-0 benzoic acid 5-phenylsulfanyl-pentyl ester 
• 923571-44-2 benzoic acid 5-methanesulfonyloxy-pentyl ester 

Downstream Products

• 5831-70-9 2-(iodomethyl)tetrahydrofuran 
• 212051-35-9 (R)-methyl 3-((4-methoxybenzyl)oxy)-2-methylpropanoate 
• 1184854-22-5 C₂₄H₃₂O₄ 
• 821-09-0 n-Pent-4-enyl alcohol 
• 1374817-37-4 (1R,6R,8S)-8-(5-((4-methoxybenzyl)oxy)pentyl)-2,9,10-trioxa-1-phosphabicyclo[4.3.1]dec-4-ene 1-oxide 
• 1018689-65-0 C₁₉H₂₅O₆P 
• 1097160-40-1 C₃₁H₃₉F₆O₈P 

Relevant articles and documents

Progress toward the total synthesis of 9β-hydroxyvertine: Construction of an advanced quinolizidine intermediate

Progress toward the total synthesis of 9β-hydroxyvertine 2 is described. Our approach involves a Petasis borono-Mannich reaction to assemble a key intermediate A, securing the correct configuration at H-9 and H-10 in the final targeted molecule. Subsequen

Mild, selective deprotection of PMB ethers with triflic acid/1,3-dimethoxybenzene

An efficient method for the cleavage of the p-methoxybenzyl protecting group of several alcohols in the presence of 0.5 equiv of trifluoromethanesulfonic acid and 1,3-dimethoxybenzene in dichloromethane at room temperature is described.

Mild preparation of alkenes from phenyl sulfides: One-pot elimination of phenylthio group via sulfilimine at ambient temperature

(Chemical Equation Presented) Various alkenes were prepared from phenyl sulfides in a one-pot manner at room temperature by converting them to the corresponding S-aminosulfonium salts with O-mesitylenesulfonylhydroxylamine, followed by treatment with pota