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294942

Sigma-Aldrich

N,N-Dicyclohexylmethylamine

97%

Synonym(s):

N-Methyldicyclohexylamine

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About This Item

Linear Formula:
(C6H11)2NCH3
CAS Number:
7560-83-0
Molecular Weight:
195.34
Beilstein/REAXYS Number:
2074991
EC Number:
231-453-4
MDL number:
MFCD00014289
UNSPSC Code:
12352100
PubChem Substance ID:
24857748
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.49 (lit.)

bp

265 °C (lit.)

density

0.912 g/mL at 25 °C (lit.)

SMILES string

CN(C1CCCCC1)C2CCCCC2

InChI

1S/C13H25N/c1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h12-13H,2-11H2,1H3

InChI key

GSCCALZHGUWNJW-UHFFFAOYSA-N

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Application

N,N-Dicyclohexylmethylamine has been employed as:
  • catalyst during O-phenylation of tertiary alcohol with organobismuth(V) compounds
  • base during Pd-catalyzed 5-endo-trig cyclization of 1-(o-bromophenyl)-2-methylprop-2-en-1-ol

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 2

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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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Sriram Kumar et al.
Nature communications, 11(1), 2960-2960 (2020-06-13)
Nucleic acid-based materials enable sub-nanometer precision in self-assembly for fields including biophysics, diagnostics, therapeutics, photonics, and nanofabrication. However, structural DNA nanotechnology has been limited to substantially hydrated media. Transfer to organic solvents commonly used in polymer and peptide synthesis results
Copper (II)-catalyzed O-phenylation of alcohols with organobismuth (V) reagents.
Sakurai N, et al.
ARKIVOC (Gainesville, FL, United States), 7, 254-264 (2007)
Heck-type reactions of allylic alcohols: Part IV:(2-Substituted)-1-indanones via 5-endo-trig cyclizations.
Zawisza AM, et al.
J. Mol. Catal. A: Chem., 283(1), 140-145 (2008)

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