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29347

Sigma-Aldrich

N-Cyclohexylaniline

≥98.0% (GC/NT)

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About This Item

Empirical Formula (Hill Notation):
C12H17N
CAS Number:
1821-36-9
Molecular Weight:
175.27
Beilstein:
2209864
EC Number:
217-344-4
MDL number:
MFCD00014284
UNSPSC Code:
12352100
PubChem Substance ID:
57648365
NACRES:
NA.22

Assay

≥98.0% (GC/NT)

form

liquid

refractive index

n20/D 1.560

density

0.996 g/mL at 20 °C (lit.)

SMILES string

C1CCC(CC1)Nc2ccccc2

InChI

1S/C12H17N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2

InChI key

TXTHKGMZDDTZFD-UHFFFAOYSA-N

Application

N-Cyclohexylaniline has been used as reagent in palladium-catalyzed amination of aromatic bromides.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H302,H315,H330,H335

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

276.8 °F - closed cup

Flash Point(C)

136 °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’.

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Mahavir Prashad et al.
The Journal of organic chemistry, 68(3), 1163-1164 (2003-02-01)
An efficient palladium-catalyzed amination of aromatic bromides with hindered N-alkyl-substituted anilines is described, either using the combination of Pd(OAc)(2) and P(t-Bu)(3) or a palladium(I) tri-tert-butylphosphine bromide dimer, [Pd(mu-Br)(t-Bu(3)P)](2), a new, commercially available, and easily handled catalyst.
Edmar Ramos Oliveira-Filho et al.
Journal of molecular microbiology and biotechnology, 28(5), 225-235 (2019-02-21)
Three different polyhydroxyalkanoate (PHA) synthase genes (Ralstonia eutropha H16, Aeromonas sp. TSM81 or Aeromonas hydrophila ATCC7966 phaC) were introduced into the chromosome of two Pseudomonas strains: a native medium-chain-length 3-polyhydroxyalkanoate (PHAMCL) producer (Pseudomonas sp. LFM046) and a UV-induced mutant strain

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