Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)-

Base Information

Chemical Name:Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)-
CAS No.:102405-33-4
Molecular Formula:C₂₀H₂₂O₂
Molecular Weight:294.393
Hs Code.:
DSSTox Substance ID:DTXSID601139004

Synonyms:DTXSID601139004;Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)-;102405-33-4

Suppliers and Price of Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)-

Supply Marketing:

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

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Chemical Property of Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)-

Chemical Property:

XLogP3:5.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:294.161979940
Heavy Atom Count:22
Complexity:383

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)C1=CC=CC(=C1)C=CC2=CC=C(C=C2)C(=O)OC
Isomeric SMILES:CC(C)(C)C1=CC=CC(=C1)/C=C/C2=CC=C(C=C2)C(=O)OC

Technology Process of Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)-

There total 3 articles about Benzoic acid, 4-[2-[3-(1,1-dimethylethyl)phenyl]ethenyl]-, methyl ester, (E)- 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:

: 1075-38-3
m-t-butyltoluene

: 102405-33-4
Methyl 4-<2-(3-tert-butylphenyl)ethenyl>benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / N-bromosuccinimide, azobisisobutyronitrile / CCl₄ / 2 h / Heating

2: 68.2 percent / benzene / 5 h / Heating

3: NaOMe / methanol

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium methylate; In methanol; tetrachloromethane; benzene;
DOI:10.1021/jm00125a027

Reference yield:

: 102405-32-3
3-tert-butylbenzyl bromide

: 102405-33-4
Methyl 4-<2-(3-tert-butylphenyl)ethenyl>benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: 68.2 percent / benzene / 5 h / Heating

2: NaOMe / methanol

With sodium methylate; In methanol; benzene;
DOI:10.1021/jm00125a027