Skip to Content
Merck
CN
All Photos(5)

Documents

D79403

Sigma-Aldrich

Bicyclohexyl

99%

Synonym(s):

1,1′-Bi(cyclohexyl), BCH, Dicyclohexyl

Sign Into View Organizational & Contract Pricing
All Photos(5)

About This Item

Linear Formula:
C6H11C6H11
CAS Number:
92-51-3
Molecular Weight:
166.30
Beilstein:
1848266
EC Number:
202-161-4
MDL number:
MFCD00003815
UNSPSC Code:
12352100
PubChem Substance ID:
24894172
NACRES:
NA.22

Quality Level

200

Assay

99%

form

liquid

autoignition temp.

473 °F

refractive index

n20/D 1.478 (lit.)

bp

227 °C (lit.)

mp

3-4 °C (lit.)

density

0.864 g/mL at 25 °C (lit.)

SMILES string

C1CCC(CC1)C2CCCCC2

InChI

1S/C12H22/c1-3-7-11(8-4-1)12-9-5-2-6-10-12/h11-12H,1-10H2

InChI key

WVIIMZNLDWSIRH-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544) , ESR1(2099)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Bicyclohexyl can be used as a reactant:      
  • To synthesize 1-azido-1,1′-bi(cyclohexane) by Mn-catalyzed oxidative azidation method using nucleophilic NaN3 as an azide source.      
  • To prepare 1-fluoro-1,1′-bicyclohexyl using elemental fluorine.   
  • In the aliphatic Friedel-Crafts reaction to prepare novel bicyclohexyl based oxygenated building block via C-H activation with aluminum trichloride and acetyl chloride.

Signal Word

Danger

Hazard Statements

H302,H304,H335,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Asp. Tox. 1 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Linbin Niu et al.
Journal of the American Chemical Society, 142(41), 17693-17702 (2020-09-18)
The selective installation of azide groups into C(sp3)-H bonds is a priority research topic in organic synthesis, particularly in pharmaceutical discovery and late-stage diversification. Herein, we demonstrate a generalized manganese-catalyzed oxidative azidation methodology of C(sp3)-H bonds using nucleophilic NaN3 as
Catherine L Lyall et al.
Organic & biomolecular chemistry, 11(9), 1468-1475 (2012-12-25)
The functionalisation of decalin by means of an "aliphatic Friedel-Crafts" reaction was reported over fifty years ago by Baddeley et al. This protocol is of current relevance in the context of C-H activation and here we demonstrate its applicability to
Lionel W Spack et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(6), 1052-1071 (2017-03-28)
The contamination of food by mineral oil hydrocarbons (MOHs) found in packaging is a long-running concern. A main source of MOHs in foods is the migration of mineral oil from recycled board into the packed food products. Consequently, the majority
Brian D Fitz et al.
Journal of chromatography. A, 1392, 82-90 (2015-03-31)
Low thermal mass gas chromatography (LTM-GC) was evaluated for rapid, high peak capacity separations with three injection methods: liquid, headspace solid phase micro-extraction (HS-SPME), and direct vapor. An Agilent LTM equipped with a short microbore capillary column was operated at

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service