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3-(1,1-biphenyl)cyclohexane is an organic compound with the molecular formula C18H18. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. 3-(1,1-biphenyl)cyclohexane is characterized by a cyclohexane ring with a biphenyl group attached at the 3-position. The biphenyl group consists of two benzene rings connected by a single bond, which gives the molecule its unique structure. 3-(1,1-biphenyl)cyclohexane is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of certain polymers and specialty chemicals. Due to its complex structure, it is important to handle 3-(1,1-biphenyl)cyclohexane with care and in accordance with proper safety protocols.

1973-15-5

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1973-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1973-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1973-15:
(6*1)+(5*9)+(4*7)+(3*3)+(2*1)+(1*5)=95
95 % 10 = 5
So 1973-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H20/c1-3-8-15(9-4-1)17-12-7-13-18(14-17)16-10-5-2-6-11-16/h1,3-4,7-9,12-14,16H,2,5-6,10-11H2

1973-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-3-phenylbenzene

1.2 Other means of identification

Product number -
Other names 3-cyclohexyl-1,1'-biphenyl

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:1973-15-5 SDS

1973-15-5Upstream product

1973-15-5Downstream Products

1973-15-5Relevant academic research and scientific papers

Using ceramic membranes for the separation of hydrogen produced by dehydrogenation of perhydro-m-terphenyl

Kalenchuk,Bogdan,Kustov

, p. 16 - 18 (2015/02/19)

The efficiency of a variety of ceramic membranes for the purification of hydrogen obtained by dehydrogenation of perhydro-m-terphenyl in a catalytic flow reactor from vapors of initial hydrocarbons and dehydrogenation products is investigated.

Regioselective cobalt-catalyzed Diels-Alder reaction towards 1,3-disubstituted and 1,2,3-trisubstituted benzene derivatives

Hilt, Gerhard,Danz, Michael

experimental part, p. 2257 - 2263 (2009/04/06)

A straightforward reaction sequence consisting of the Wittig olefmation of aldehydes utilizing allyltriphenylphosphonium bromide for the generation of 1-substituted 1,3-dienes, cobalt-catalyzed neutral Diels-Alder reaction with terminal and internal alkyn

Method for producing biaryl compound

-

, (2008/06/13)

There is disclosed a method for producing a biaryl compound of formula (I): wherein R1 is the same or different and independently denotes a substituted or unsubstituted hydrocarbon group or the like, A and B denote an aromatic hydrocarbon ring having from 6 to 14 carbon atoms or the like, k and m independently denote an integer of from 0 to 5, and 1 denotes an integer of 1 or 2, which method is characterized by reacting an aromatic compound of formula (II): wherein R1, k and l denote the same as defined above, and X1 denotes a leaving group, with a Grignard reagent of formula (III): (R2). 9MgX2 (IIIg) wherein R2, B, and m denote the same as defined above and X2 denotes chlorine or the like, in the presence of a cyclic ether, or an acyclic ether having two or more ether oxygens in the molecule and a nickel catalyst.

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