207120-79-4

Basic information

• Product Name: Benzene, 1-methoxy-4-[[(3-methyl-2-butenyl)oxy]methyl]-
• CAS NO: 207120-79-4
• Molecular Formula: C13H18O2
• Molecular Weight: 206.285
• Mol File: 207120-79-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methoxy-4-[[(3-methyl-2-butenyl)oxy]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-4-[[(3-methyl-2-butenyl)oxy]methyl]-(207120-79-4)
• EPA Substance Registry System: Benzene, 1-methoxy-4-[[(3-methyl-2-butenyl)oxy]methyl]-(207120-79-4)

Safety Data

• Hazardous Substances Data: 207120-79-4(Hazardous Substances Data)

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 556-82-1 3-methyl-2-buten-1-ol 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 197227-70-6 (2E)-4-[(4-methoxybenzyl)oxy]-2-methylbut-2-enal 
• 612090-74-1 (2Z)-4-(4-methoxybenzyloxy)-2-methyl-2-butenal 
• 1180481-32-6 C₂₁H₃₆O₂Si 
• 688762-95-0 3,5-dioxo-hexanoic acid (E)-(S)-8-(4-methoxy-benzyloxy)-2,6-dimethyl-oct-6-enyl ester 
• 688762-45-0 2-[(E)-6-(4-methoxy-benzyloxy)-4-methyl-hex-4-enyl]-2-methyl-malonic acid diethyl ester 
• 688762-53-0 acetic acid (E)-(S)-8-(4-methoxy-benzyloxy)-2,6-dimethyl-oct-6-enyl ester 
• 688762-41-6 (E)-8-(4-methoxy-benzyloxy)-2,6-dimethyl-oct-6-enoic acid ethyl ester 
• 688762-49-4 (E)-8-(4-methoxybenzyloxy)-2,6-dimethyl-oct-6-en-1-ol 
• 688762-74-5 (E)-8-(4-methoxybenzyloxy)-2,6-dimethyl-oct-6-en-1-ol 
• 688762-47-2 (E)-8-(4-methoxybenzyloxy)-2,6-dimethyl-oct-6-en-1-ol 
• 688762-37-0 (E)-6-(4-methoxy-benzyloxy)-4-methyl-hex-4-enoic acid ethyl ester 
• 688762-43-8 1-((E)-6-iodo-3-methyl-hex-2-enyloxymethyl)-4-methoxy-benzene 
• 688762-39-2 (E)-6-(4-methoxy-benzyloxy)-4-methyl-hex-4-en-1-ol 
• 145369-57-9 1-p-methoxybenzyloxy-3-methylbut-3-en-2-one 

Relevant articles and documents

Synthesis of the C(18)-C(34) fragment of amphidinolide C and the C(18)-C(29) fragment of amphidinolide F

A convergent synthesis of the C(18)-C(34) fragment of amphidinolide C and the C(18)-C(29) fragment of amphidinolide F is reported. The approach involves the synthesis of the common intermediate tetrahydrofuranyl-β- ketophosphonate via cross metathesis, Pd

Total synthesis of milbemycins: A synthesis of (6R)-6-hydroxy-3,4- dihydromilbemycin E

Following studies using benzyloxymethyl isopropenyl ketone 5 and ethyl 3-(3-furyl)-3-oxopropanoate 6, Robinson reactions between aryloxymethyl isopropenyl ketones 19 and 5 and ethyl 3-(2-trimethylsilyl-3-furyl)-3- oxopropanoate 20 were found to be stereos

Study of the stability of carbocations by chlorosulfonyl isocyanate reaction with ethers

The stability order of various alkyl, allyl, and benzyl carbocations was investigated using the novel technique for comparing the stability of carbocations in solution developed by using a simple CSI reaction with various ethers. The p-methoxycinnamyl carbocation was the most stable in our reaction system and the next stable carbocation was the p-methoxybenzyl carbocation. The stability of the other carbocations decreased with methacryl, t-butyl, cinnamyl, acryl, benzyl, 2° and allyl carbocations in that order.