Saltar al contenido
Merck

D79403

Sigma-Aldrich

Bicyclohexyl

99%

Sinónimos:

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

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
C6H11C6H11
Número de CAS:
Peso molecular:
166.30
Beilstein/REAXYS Number:
1848266
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

¿Está buscando productos similares? Visita Guía de comparación de productos

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.

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

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
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
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
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

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico