1,4-Di-tert-pentylbenzene

Base Information

• Chemical Name: 1,4-Di-tert-pentylbenzene
• CAS No.: 3373-10-2
• Molecular Formula: C16H26
• Molecular Weight: 218.382
• Hs Code.: 2902909090
• European Community (EC) Number: 222-156-0
• DSSTox Substance ID: DTXSID8062999
• Nikkaji Number: J105.382E
• Wikidata: Q81990418
• Mol file: 3373-10-2.mol

Synonyms:1,4-Di-tert-pentylbenzene;3373-10-2;Benzene, p-di-tert-pentyl-;p-Di-tert-amylbenzene;p-Di-tert-pentylbenzene;1,4-Dimethyl-pentylbenaen;1,4-Di(tert-pentyl)benzene;DTXSID8062999;EINECS 222-156-0;1,4-bis(1,1-dimethylpropyl)-benzene;Benzene, 1,4-bis(1,1-dimethylpropyl)-

Chemical Property of 1,4-Di-tert-pentylbenzene

Chemical Property:

• Vapor Pressure: 0.00691mmHg at 25°C
• Boiling Point: 279.2°Cat760mmHg
• Flash Point: 121.4°C
• PSA: 0.00000
• Density: 0.853g/cm³
• LogP: 5.06180
• XLogP3: 6.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 4
• Exact Mass: 218.203450829
• Heavy Atom Count: 16
• Complexity: 180

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 1,4-Di-tert-pentylbenzene

There total 9 articles about 1,4-Di-tert-pentylbenzene 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:

isopentyl ether (544-01-4) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → tery-amylbenzene (2049-95-8) + 1,4-di-tert-pentyl-benzene (3373-10-2)

Guidance literature:

With boron trifluoride; at 150 ℃; under 9561.6 Torr;

DOI:10.1021/ja01268a038

Reference yield:

2-Methyl-1-butene (563-46-2) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → tery-amylbenzene (2049-95-8) + 1,4-di-tert-pentyl-benzene (3373-10-2)

Guidance literature:

With sulfuric acid;

DOI:10.1021/ja01271a508 DOI:10.1021/ja01269a035 DOI:10.1021/ja01287a002

Reference yield:

2-methyl-but-2-ene (513-35-9) + benzene (71-43-2,26181-88-4,54682-86-9,13967-78-7,174973-66-1) → tery-amylbenzene (2049-95-8) + 1,4-di-tert-pentyl-benzene (3373-10-2)

Guidance literature:

With sulfuric acid;

DOI:10.1021/ja01271a508 DOI:10.1021/ja01269a035 DOI:10.1021/ja01287a002

upstream raw materials:

2-Methyl-1-butene

benzene

tert-Amyl alcohol

2-methyl-but-2-ene

Downstream raw materials:

tery-amylbenzene