4-[(4-Ethenylphenyl)methoxy]butan-1-OL

Base Information

• Chemical Name: 4-[(4-Ethenylphenyl)methoxy]butan-1-OL
• CAS No.: 92035-97-7
• Molecular Formula: C13H18O2
• Molecular Weight: 206.285
• DSSTox Substance ID: DTXSID20594113
• Nikkaji Number: J798.576B
• Wikidata: Q82488849
• Mol file: 92035-97-7.mol

Synonyms:92035-97-7;1-Butanol, 4-[(4-ethenylphenyl)methoxy]-;4-[(4-ETHENYLPHENYL)METHOXY]BUTAN-1-OL;SCHEMBL4903352;DTXSID20594113;ZCVDFTDKYCFDBG-UHFFFAOYSA-N;4-Hydroxy-1(4'-vinylbenzyloxy)butane;4-Hydroxy-1-(4-vinylbenzyloxy)butane

Chemical Property of 4-[(4-Ethenylphenyl)methoxy]butan-1-OL

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 7
• Exact Mass: 206.130679813
• Heavy Atom Count: 15
• Complexity: 160

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC1=CC=C(C=C1)COCCCCO

Technology Process of 4-[(4-Ethenylphenyl)methoxy]butan-1-OL

There total 4 articles about 4-[(4-Ethenylphenyl)methoxy]butan-1-OL which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

1-({4-[(tert-butyl)dimethylsilyloxy]butoxy}methyl)-4-ethenylbenzene (434936-48-8) → 4-(4-ethenylbenzyloxy)butan-1-ol (92035-97-7)

Guidance literature:

With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 12h;

DOI:10.1002/1522-2675(200201)85:1<352::AID-HLCA352>3.0.CO;2-D

Reference yield: 86.0%

Butane-1,4-diol (110-63-4) + 4-Vinylbenzyl chloride (1592-20-7,29296-32-0) → 4-(4-ethenylbenzyloxy)butan-1-ol (92035-97-7)

Guidance literature:

With sodium hydroxide; water; at 70 ℃; for 24h;

DOI:10.1002/adsc.200600376

Reference yield:

C21H24O3 (1013655-39-4) → phenylacetic acid (103-82-2) + 4-(4-ethenylbenzyloxy)butan-1-ol (92035-97-7)

Guidance literature:

With phosphate buffer; at 37 ℃; pH=8; Kinetics;

DOI:10.1002/adsc.200600376

upstream raw materials:

Butane-1,4-diol

1-(2-chloroethyl)-4-(chloromethyl)benzene

1-({4-[(tert-butyl)dimethylsilyloxy]butoxy}methyl)-4-ethenylbenzene

4-Vinylbenzyl chloride

Downstream raw materials:

1-{[(tert-butyl)diphenylsilyloxy]methyl}-4-{[4-(4-ethenylbenzyloxy)butoxy]methyl}benzene

C₂₁H₂₄O₃

2-methyl-2-[4-(4-vinyl-benzyloxy)-butyl]-propanedioyl dichloride

2-methyl-2-[4-(4-vinyl-benzyloxy)-butyl]-malonic acid