Welcome to LookChem.com Sign In|Join Free

CAS

  • or
[trans(trans)]-4,4'-bis(4-pentylcyclohexyl)biphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79832-84-1

Post Buying Request

79832-84-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

79832-84-1 Usage

Chemical compound

BPCH is a chemical compound that belongs to the family of biphenyls.

Liquid crystal material

It is used in the production of liquid crystal displays (LCDs) for electronic devices such as smartphones, televisions, and computer monitors.

Thermal stability

BPCH has excellent thermal stability, making it suitable for high-performance applications.

Mechanical properties

It also has excellent mechanical properties, which contribute to its performance in electronic devices.

Molecular structure

BPCH's unique molecular structure allows it to exhibit nematic and smectic liquid crystalline phases, which are essential for the functioning of LCD displays.

Potential applications

BPCH has attracted attention for its potential as a dielectric material in organic electronic devices and as a component in advanced materials for drug delivery and medical imaging.

Check Digit Verification of cas no

The CAS Registry Mumber 79832-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79832-84:
(7*7)+(6*9)+(5*8)+(4*3)+(3*2)+(2*8)+(1*4)=181
181 % 10 = 1
So 79832-84-1 is a valid CAS Registry Number.

79832-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-pentylcyclohexyl)-4-[4-(4-pentylcyclohexyl)phenyl]benzene

1.2 Other means of identification

Product number -
Other names EINECS 279-322-0

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:79832-84-1 SDS

79832-84-1Downstream Products

79832-84-1Relevant articles and documents

Novel Liquid Crystalline Compounds Containing Bicyclo[3.1.0]hexane Core Units

Kozhushkov, Sergei I.,Langer, Rainer,Yufit, Dmitrii S.,Howard, Judith A. K.,Schill, Heiko,Demus, Dietrich,Miyazawa, Kazutoshi,De Meijere, Armin

, p. 289 - 303 (2007/10/03)

Additions of ethyl or tert-butyl diazoacetates to 4-substituted cyclopentenes 6 and 17 under dirhodium tetraacetate/tetraoctanoate catalysis led to mixtures of tert-butyl endo,exo- and exo,exo-3-carboxyl(aryl)bicyclo[3.1.0]hexane-6-carboxylates 7 and 18 in yields of 54-90% from which exo,exo-diastereomers were isolated in yields of 39-63%. Diester exo,exo-7 was saponified and converted into diaryl diesters exo,exo-9a, b in overall yields of 42 and 46%, respectively. The esters exo,exo-18 were reduced to the corresponding hydroxymethyl derivatives, these were transformed to the iodomethyl compounds which in turn were coupled with various alkylmagnesium halides, via Li2CuCl4 catalysis, to give 3-aryl-6-alkylbicyclo[3.1.0]hexyl derivatives exo,exo-21 in overall yields of 72-83%. Fluorinated 3-(2-arylethyl)-6-pentylbicyclo[3.1.0]hexane exo,exo-32 could be prepared in five steps from 4-ethoxy-2,3-difluorobenzaldehyde 26a adopting essentially the same synthetic strategy, but in an overall yield of only 8%, and 6-(4-cyanophenyl)-3-pentylbicyclo[3.1.0]hexane exo,exo-38b was obtained by Pd(OAc)2 catalyzed cyclopropanation of 4-pentylcyclopentene 34b with (4-cyanophenyl)diazomethane 36b in 29% yield. A comparison of the liquid crystalline properties of these newly prepared compounds containing a bicyclo[3.1.0]hexane core with those of the known analogous compounds with a cyclohexane fragment shows that as a rule, a bicyclo[3.1.0]hexane moiety decreases the transition temperature, while the dielectric (Δε) and optical (Δn) anisotropies are comparable. However, the bicyclo[3.1.0]hexane unit has a poorer mesogenic potential, Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

Synthesis of Mesogenic Compounds, Catalyzed by Metal Complexes. II. A New Method of Synthesis of 4,4'-Dialkylbiphenyls

Bumagin, N. A.,Luzikova, E. V.,Beletskaya, I. P.

, p. 1487 - 1491 (2007/10/03)

A new method for the synthesis of 4,4'-dialkylbiphenyls containing both n-alkyl- and 4-trans-n-alkylcyclohexyl substituents, based on highly selective reactions of monoalkylation and monoacylation of 1,4-dibromobenzene in the presence of palladium complexes is developed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 79832-84-1