4-(1-Ethylpentyl)phenol

Base Information

Chemical Name:4-(1-Ethylpentyl)phenol
CAS No.:6465-74-3
Molecular Formula:C₁₃H₂₀O
Molecular Weight:192.301
Hs Code.:
DSSTox Substance ID:DTXSID901029327
Nikkaji Number:J870.501A

Synonyms:4-(1-Ethylpentyl)phenol;VVMIIKFOWHZTCV-UHFFFAOYSA-N;DTXSID901029327;6465-74-3;NS00134460

Suppliers and Price of 4-(1-Ethylpentyl)phenol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of 4-(1-Ethylpentyl)phenol

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:192.151415257
Heavy Atom Count:14
Complexity:136

Purity/Quality:: 99.9% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC(CC)C1=CC=C(C=C1)O

Technology Process of 4-(1-Ethylpentyl)phenol

There total 5 articles about 4-(1-Ethylpentyl)phenol 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: 48.0%

: 106-35-4
heptan-3-one

: 108-95-2,27073-41-2
phenol

: 6465-74-3
3-(p-hydroxyphenyl)heptane

Guidance literature:: With Al⁺-exchanged montmorillonite; at 100 ℃; for 48h;
DOI:10.1246/cl.1996.59

Reference yield:

: 17403-85-9
4-<1-Ethyl-penten-(1)-yl>-anisol

: 6465-74-3
3-(p-hydroxyphenyl)heptane

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd-C / ethanol

2: aq. HBr / acetic acid

With hydrogen bromide; hydrogen; palladium on activated charcoal; In ethanol; acetic acid;
DOI:10.1039/j39670002281

Reference yield:

: 121-97-1
4-Methoxypropiophenone

: 6465-74-3
3-(p-hydroxyphenyl)heptane

Guidance literature:: Multi-step reaction with 3 steps

1: (i) Et₂O, (ii) (heating)

2: H₂ / Pd-C / ethanol

3: aq. HBr / acetic acid

With hydrogen bromide; hydrogen; palladium on activated charcoal; In ethanol; acetic acid;
DOI:10.1039/j39670002281