p-Decyloxyphenol

Base Information

• Chemical Name: p-Decyloxyphenol
• CAS No.: 35108-00-0
• Molecular Formula: C16H26 O2
• Molecular Weight: 250.381
• Hs Code.: 2909500000
• DSSTox Substance ID: DTXSID70394483
• Nikkaji Number: J1.661.685K
• Wikidata: Q82193895
• Mol file: 35108-00-0.mol

Synonyms:p-Decyloxyphenol;4-(decyloxy)phenol;35108-00-0;4-decoxyphenol;4-(decyloxy)benzenol;4-decyloxyphenol;4-decy-loxyphenol;4-DECYLOXY-PHENOL;SCHEMBL1835315;DTXSID70394483;MFCD00224992;STK050813;AKOS001483002;12N-236

Chemical Property of p-Decyloxyphenol

Chemical Property:

• Vapor Pressure: 5.21E-06mmHg at 25°C
• Melting Point: 69-69.5 °C
• Boiling Point: 370.4°Cat760mmHg
• PKA: 10.33±0.15(Predicted)
• Flash Point: 154.5°C
• PSA: 29.46000
• Density: 0.961g/cm³
• LogP: 4.91170
• XLogP3: 6.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 250.193280068
• Heavy Atom Count: 18
• Complexity: 174

Purity/Quality:

99% ^*data from raw suppliers

4-(Decyloxy)benzenol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCOC1=CC=C(C=C1)O
• Uses: 4-(Decyloxy)phenol is used as a reactant in the preparation of liquid crystal halogen-bond dimers with substituted pyridines.

Technology Process of p-Decyloxyphenol

There total 24 articles about p-Decyloxyphenol 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: 96.0%

4-decyloxyphenylboronic acid (147222-99-9) → 4-decyloxyphenol (35108-00-0)

Guidance literature:

With oxygen; N-ethyl-N,N-diisopropylamine; In ethanol; toluene; Irradiation; Flow reactor;

DOI:10.1039/d0ra10147h

Reference yield: 94.0%

4-(decyloxy)benzaldehyde (24083-16-7) + C27H32N6O4 → 4-decyloxyphenol (35108-00-0) + p-decyloxybenzoic acid (5519-23-3) + (9H-fluoren-9-yl)methyl ((R)-1-(((S)-1-amino-6-formamido-1-oxohexan-2-yl)amino)-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl)carbamate

Guidance literature:

In aq. phosphate buffer; N,N-dimethyl-formamide; at 25 ℃; for 48h; pH=7.0; chemoselective reaction;

DOI:10.1039/c6cc09555k

Reference yield: 93.0%

4-(decyloxy)benzaldehyde (24083-16-7) + C27H27ClFN3O3 → 4-decyloxyphenol (35108-00-0) + p-decyloxybenzoic acid (5519-23-3) + (9H-fluoren-9-yl)methyl (S)-(1-((3-chloro-4-fluorophenyl) amino)-6-formamido-1-oxohexan-2-yl)carbamate

Guidance literature:

In aq. phosphate buffer; N,N-dimethyl-formamide; at 25 ℃; for 48h; pH=7.0; chemoselective reaction;

DOI:10.1039/c6cc09555k

upstream raw materials:

decyl p-toluenesulfonate

sodium 4-hydroxybenzen-1-olate

1-Decanol

hydroquinone

Downstream raw materials:

Benzene-1,2,4-tricarboxylic acid tris-(4-decyloxy-phenyl) ester

4-decyloxyphenyl 4-(benzyloxy)benzoate

4-decyloxyphenyl 4-decyloxybenzoate

(2R,3S)-(-)-4-decyloxyphenyl-3--oxirane-2-carboxylate