1530-05-8

Usage

Uses

Used in Chemical Synthesis:
1,1-Diphenylheptane is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to be a valuable component in the synthesis of a range of chemical products.
Used in Research and Laboratory Settings:
Due to its properties and reactivity, 1,1-Diphenylheptane is also utilized in research and laboratory settings for the study and development of new chemical processes and compounds.

InChI:InChI=1/C19H24/c1-2-3-4-11-16-19(17-12-7-5-8-13-17)18-14-9-6-10-15-18/h5-10,12-15,19H,2-4,11,16H2,1H3

Upstream product

• 688-82-4 1,1-diethoxyheptane 
• 1530-20-7 1,1-diphenyl-1-heptene 
• 821-25-0 1,1-dichloroheptane 
• 71-43-2 benzene 
• 75-77-4 chloro-trimethyl-silane 
• 74-85-1 ethene 
• 881-42-5 diphenylmethyllithium 
• 52247-11-7 1,1-diphenylheptan-1-ol 
• 1671-75-6 Heptanophenone 
• 530-48-3 1,1-Diphenylethylene 
• 1078-71-3 heptylbenzene 
• 591-50-4 iodobenzene 
• 5558-70-3 2,2-diphenyloctanenitrile 

Downstream Products

• 175391-09-0 1,1-Bis(4-t-butylphenyl)heptane 
• 177478-72-7 1,1-bis(4-(4-nitrobenzoyl)phenyl)heptane 

Relevant academic research and scientific papers

C(sp3)-H selective benzylic borylation by in situ reduced ultrasmall Ni species on CeO2

Herein, we report that highly dispersed Ni hydroxide species supported on CeO2 act as an efficient heterogeneous catalyst for the selective borylation of benzylic C(sp3)-H bonds of alkylarenes including secondary derivatives, using pinacolborane as the bo

Metal-Organic Framework with Dual Active Sites in Engineered Mesopores for Bioinspired Synergistic Catalysis

Here we report the design of an enzyme-inspired metal-organic framework (MOF), 1-OTf-Ir, by installing strong Lewis acid and photoredox sites in engineered mesopores. Al-MOF (1), with mixed 2,2′-bipyridyl-5,5-dicarboxylate (dcbpy) and 1,4-benzenediacrylat

Polyethylene glycol mediated reductive decyanation of diphenylacetonitrile moderately enhanced by microwave heating

An efficient and clean procedure for the preparation of alkyldiphenylmethanes and 4,4-diphenylbutylamines from their corresponding nitriles by using sodium hydroxide-polyethylene glycol reagent system in a domestic microwave oven is described. The products are isolated by simple aqueous work up in excellent yields.

Diamino compounds and methods for preparing them

An object of the invention is to propose diamino compounds expressed by the following general formula (1) which are suitable to obtain a raw material, a polyimide resin, for a liquid crystal aligning film without any image sticking and with a high voltage holding ratio at from a low temperature to a high temperature as well as the preparation thereof: STR1

Carbanion Rearrangements by Intramolecular 1,ω Proton Shifts, IV. The Reaction of ω,ω-Diphenylalkyllithium Compounds: Proof for an Intramolecular Transmetallation Reaction by Crossover Experiments Using Isotopic Labelled Starting Material

3,3-Diphenylpropyllithium (2) and 2-(9-fluorenyl)ethyllithium (43) do not show a 1,3 proton shift but splitt off ethylene.On the other hand 4,4-diphenylbutyllithium (19) in diethyl ether can be forced to rearrange to 1,1-diphenylbutyllithium (18) by the addition of THF.The half reaction time for this 1,4 proton shift was found to be about 4 minutes.Proof for the intramolecular character of this transmetallation reaction was obtained by crossover experiments with specifically deuterated starting material.The 1,5 proton shift with 5,5-diphenylpentyllithium (12) occurs considerably slower than the 1,4 shift with 4,4-diphenylbutyllithium (19).The rearrangement also takes place in pure diethyl ether although with a half reaction time of about 2 days.Only 3-(9-fluorenyl)propyllithium (41) in diethyl ether spontaneously shows rearrangement already at -30 deg C, whereby 9-propyl-9-fluorenyllithium (42) is formed by a 1,4 proton shift.A 1,ω phenyl migration according to Grovenstein-Zimmerman in no case could be observed.