C₂₈H₂₄O

Base Information

Chemical Name:C₂₈H₂₄O
CAS No.:83248-33-3
Molecular Formula:C₂₈H₂₄O
Molecular Weight:376.498
Hs Code.:

Synonyms:

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

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Chemical Property of C₂₈H₂₄O

Chemical Property:

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Technology Process of C₂₈H₂₄O

There total 4 articles about C₂₈H₂₄O 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:

: 72292-01-4
(2-(2-methylphenyl)ethene-1,1-diyl)dibenzene

: 83248-33-3
C₂₈H₂₄O

Guidance literature:: Multi-step reaction with 2 steps

1: 30 percent / bromine / CCl₄

2: 99 percent Chromat_. / AgOTf, 2,6-di-tert-butyl-4-methylpyridine / 24 h / 150 °C

With 2,6-di-tert-butyl-4-methylpyridine; bromine; silver trifluoromethanesulfonate; In tetrachloromethane;
DOI:10.1021/jo00146a033

Reference yield:

: 72292-00-3
1,1-Diphenyl-2-(2-tolyl)-ethanol

: 83248-33-3
C₂₈H₂₄O

Guidance literature:: Multi-step reaction with 3 steps

1: 85percent H₃PO₄ / 2 h / 130 °C

2: 30 percent / bromine / CCl₄

3: 99 percent Chromat_. / AgOTf, 2,6-di-tert-butyl-4-methylpyridine / 24 h / 150 °C

With 2,6-di-tert-butyl-4-methylpyridine; phosphoric acid; bromine; silver trifluoromethanesulfonate; In tetrachloromethane;
DOI:10.1021/jo00146a033

Reference yield:

: phenylmagnesium bromide

: 83248-33-3
C₂₈H₂₄O

Guidance literature:: Multi-step reaction with 4 steps

1: diethyl ether

2: 85percent H₃PO₄ / 2 h / 130 °C

3: 30 percent / bromine / CCl₄

4: 99 percent Chromat_. / AgOTf, 2,6-di-tert-butyl-4-methylpyridine / 24 h / 150 °C

With 2,6-di-tert-butyl-4-methylpyridine; phosphoric acid; bromine; silver trifluoromethanesulfonate; In tetrachloromethane; diethyl ether;
DOI:10.1021/jo00146a033