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2,5-Diphenylhexane is an organic compound with the molecular formula C18H22. It is a colorless, crystalline solid that is insoluble in water but soluble in organic solvents. 2,5-Diphenylhexane is characterized by a hexane chain with two phenyl groups attached at the 2nd and 5th carbon atoms. It is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, 2,5-diphenylhexane can also be employed as a ligand in coordination chemistry and as a building block in the construction of more complex organic molecules.

3548-85-4

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3548-85-4 Usage

Hydrocarbon structure

Six-carbon chain with two phenyl groups attached at the 2 and 5 positions

Polarity

Nonpolar

Solubility

Insoluble in water, soluble in nonpolar solvents such as benzene and diethyl ether

Uses

Organic synthesis, component of some fragrances and perfumes

Molecular weight

238.37 g/mol

Melting point

90-92°C

Stability

Relatively stable under normal conditions

Health hazards

Not known to pose any significant health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 3548-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3548-85:
(6*3)+(5*5)+(4*4)+(3*8)+(2*8)+(1*5)=104
104 % 10 = 4
So 3548-85-4 is a valid CAS Registry Number.

3548-85-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylhexan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names rac-2,5-diphenylhexane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3548-85-4 SDS

3548-85-4Downstream Products

3548-85-4Relevant academic research and scientific papers

Homocoupling of iodoarenes and bromoalkanes using photoredox gold catalysis: A light enabled Au(III) reductive elimination

Tran, Huy,McCallum, Terry,Morin, Mathieu,Barriault, Louis

supporting information, p. 4308 - 4311 (2016/09/09)

The formation of homocoupled alkane byproducts have been identified in the reduction of bromoalkanes via photoredox gold catalysis with dimeric Au(I) complexes. This prompted further investigation into the mechanism of formation of these byproducts and the diversity of C-X bonds amenable to this transformation. Examples were found when considering bromoalkanes while a wide variety of iodoarenes underwent this process in good to excellent yields. The light enabled homocoupling of iodoarenes made possible by photoredox gold catalysis is reported.

PROCESS FOR PRODUCING CUMENE

-

Page/Page column 4-5, (2008/06/13)

A process for the production of cumene, which comprises producing cumene from cumyl alcohol and hydrogen with a dehydration catalyst and a hydrogenation catalyst, wherein the dehydration catalyst and hydrogenation catalyst are alternately packed so as to form n layers (n is an integer of 3 or more) or are packed as a mixture thereof in a reactor.

Silver-catalyzed alkyl-alkyl homo-coupling of Grignard reagents

Nagano, Takashi,Hayashi, Tamio

, p. 1152 - 1153 (2007/10/03)

Oxidative homo-coupling of alkyl Grignard reagents possessing β-hydrogens proceeded with high selectivity in the presence of silver tosylate (AgOTs) as a catalyst (1 mol %) and 1,2-dibromoethane as a reoxidant. Copyright

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