2,4,6-Triisopropylphenol

Base Information

• Chemical Name: 2,4,6-Triisopropylphenol
• CAS No.: 2934-07-8
• Molecular Formula: C15H24 O
• Molecular Weight: 220.355
• Hs Code.: 2907199090
• European Community (EC) Number: 220-907-7
• DSSTox Substance ID: DTXSID1041340
• Nikkaji Number: J155.461A
• Wikidata: Q2162855
• Mol file: 2934-07-8.mol

Synonyms:2,4,6-Triisopropylphenol;2934-07-8;Phenol, 2,4,6-tris(1-methylethyl)-;AI3-11243;2,4,6-tri(propan-2-yl)phenol;2,4,6-Tris(1-methylethyl)phenol;starbld0016488;2.4.6-Triisopropylphenol;SCHEMBL94533;2,4,6 - triisopropylphenol;2,4,6-Triisopropylphenol #;DTXSID1041340;HVFKKINZIWVNQG-UHFFFAOYSA-;2,4,6-tris(propan-2-yl)phenol;EINECS 220-907-7;AKOS022506458;AS-81266;FT-0697119;Q2162855

Chemical Property of 2,4,6-Triisopropylphenol

Chemical Property:

• Vapor Pressure: 0.00324mmHg at 25°C
• Boiling Point: 274.4°Cat760mmHg
• Flash Point: 123.3°C
• PSA: 20.23000
• Density: 0.925g/cm³
• LogP: 4.76240
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 220.182715385
• Heavy Atom Count: 16
• Complexity: 190

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 2,4,6-Triisopropylphenol

There total 39 articles about 2,4,6-Triisopropylphenol 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: 93.0%

C20H28O4 → 2,4,6-triisopropylphenol (2934-07-8)

Guidance literature:

With methylamine; In ethanol; at 25 ℃; for 1h;

DOI:10.1021/acs.orglett.5b00953

Reference yield: 82.0%

(2,4,6-triisopropylphenyl)magnesium bromide (108894-99-1) → 2,4,6-triisopropylphenol (2934-07-8)

Guidance literature:

With air; In tetrahydrofuran; at -25 ℃; for 0.0566667h; under 12929 Torr; Green chemistry;

DOI:10.1002/anie.201310572

Reference yield: 78.0%

C21H38OSi → 2,4,6-triisopropylphenol (2934-07-8)

Guidance literature:

With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 - 25 ℃; for 3h;

DOI:10.1021/acs.orglett.8b00287

upstream raw materials:

n-heptane

isopropyl-(2,4,6-triisopropyl-phenyl)-ether

n-pentylsodium

isopropoxybenzene

Downstream raw materials:

2-(1-methylethyl)phenol

2,4-diisopropylphenol

isopropyl diphenyl phosphate

diphenyl-p-isopropylphenyl phosphate

Refernces

• 1、 Mai, Fuhang,Cui, Kai,Wen, Zhe,Wu, Kai,Yan, Fei,Chen, Mengmeng,Chen, Hong,Li, Yongdan. "Highly selective conversion of guaiacol to: Tert -butylphenols in supercritical ethanol over a H2WO4 catalyst". . p. 2764 - 2771. Retrieved 2019/02/01.
• 2、 -. "Method for preparing hydrocarbyl phenol by catalytic conversion of phenolic compound in presence of molybdenum-based catalyst". Paragraph 0042-0043; 0070. . Retrieved 2018/04/02.