1-Benzyl-4-tert-butylbenzene

Base Information

Chemical Name:1-Benzyl-4-tert-butylbenzene
CAS No.:16251-99-3
Molecular Formula:C17H20
Molecular Weight:224.346
Hs Code.:
DSSTox Substance ID:DTXSID90454316
Nikkaji Number:J376.986K
Wikidata:Q82275771
Mol file:16251-99-3.mol

Synonyms:1-benzyl-4-tert-butylbenzene;1-benzyl-4-tert-butyl-benzene;p-t-butyldiphenylmethane;16251-99-3;Benzene, 1-(1,1-dimethylethyl)-4-(phenylmethyl)-;DTXSID90454316

Suppliers and Price of 1-Benzyl-4-tert-butylbenzene

Supply Marketing:

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

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Chemical Property of 1-Benzyl-4-tert-butylbenzene

Chemical Property:

XLogP3:6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:224.156500638
Heavy Atom Count:17
Complexity:209

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)CC2=CC=CC=C2

Technology Process of 1-Benzyl-4-tert-butylbenzene

There total 44 articles about 1-Benzyl-4-tert-butylbenzene 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: 99.0%

: 22679-54-5
4-tert-butylbenzophenone

: 16251-99-3
1-benzyl-4-tert-butylbenzene

Guidance literature:: With tris(pentafluorophenyl)borate; hydrogen; In toluene; at 70 ℃; for 12h; under 45603.1 Torr; Molecular sieve;
DOI:10.1002/anie.201503087

Reference yield: 99.0%

: 1602929-09-8
N,N-ditosyl-4-tert-butylbenzylamine

: 98-80-6
phenylboronic acid

: 16251-99-3
1-benzyl-4-tert-butylbenzene

Guidance literature:: With tetrakis(acetonitrile)palladium(II) tetrafluoroborate; potassium carbonate; bis[2-(diphenylphosphino)phenyl] ether; In N,N-dimethyl-formamide; at 60 ℃; for 3h; Inert atmosphere;
DOI:10.1021/jo500462n

Reference yield: 96.0%

: 5-((4-(tert-butyl)phenyl)(phenyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dione

: 2033-24-1
cycl-isopropylidene malonate

: 16251-99-3
1-benzyl-4-tert-butylbenzene

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 24h; under 760.051 Torr;
DOI:10.1002/adsc.201600535