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467952

Sigma-Aldrich

1-Bromo-2-cyclohexylethane

98%

Synonym(s):

2-Cyclohexylethyl bromide

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About This Item

Linear Formula:
C6H11CH2CH2Br
CAS Number:
1647-26-3
Molecular Weight:
191.11
EC Number:
216-712-1
MDL number:
MFCD00019398
UNSPSC Code:
12352100
PubChem Substance ID:
24870450
NACRES:
NA.22
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Quality Level

200

Assay

98%

refractive index

n20/D 1.49 (lit.)

bp

209 °C (lit.)

density

1.221 g/mL at 25 °C (lit.)

functional group

bromo

SMILES string

BrCCC1CCCCC1

InChI

1S/C8H15Br/c9-7-6-8-4-2-1-3-5-8/h8H,1-7H2

InChI key

JRQAAYVLPPGEHT-UHFFFAOYSA-N

General description

1-Bromo-2-cyclohexylethane is a halogenated hydrocarbon. Reaction of 1-bromo-2-cyclohexylethane with pillar[5]arene has been investigated.[1]

Application

1-Bromo-2-cyclohexylethane may be used in the synthesis of 2-cyclohexylethyloxy-4-nitroaniline.[2]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4043
BCCC6234
BCBT9857
BCBQ0188V
BCBP4872V

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Min Wang et al.
Bioorganic & medicinal chemistry letters, 17(2), 332-336 (2006-11-11)
Aromatase is a particularly good target in the treatment of estrogen receptor positive breast cancer. Novel carbon-11 labeled sulfonanilide analogues, N-[11C]methyl-N-(2-alkyloxy-4-nitrophenyl)-methanesulfonamides ([11C]3a-f, alkyl=propyl, isopropyl, 1-ethyl-propyl, cyclopentyl, cyclohexyl, and cyclohexylethyl), were designed and synthesized as potential PET agents for imaging of
Isomerization of alkyl branched alkynoic acids.
Abrams S R.
Canadian Journal of Chemistry, 64(3), 457-463 (1986)
Peter J Cragg et al.
Chemical Society reviews, 41(2), 597-607 (2011-08-02)
Pillar[5]arenes are [1(5)]paracyclophane derivatives consisting of 1,4-disubstituted hydroquinones linked by methylene bridges in the 2,5-positions. The first report of these novel macrocycles was in 2008, when 1,4-dimethoxypillar[5]arene was prepared in 22% yield, and subsequent improvements in synthetic methods have allowed

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