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D80401

Sigma-Aldrich

Dicyclohexyl ketone

98%

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About This Item

Linear Formula:
(C6H11)2CO
CAS Number:
119-60-8
Molecular Weight:
194.31
EC Number:
204-336-0
MDL number:
MFCD00040417
UNSPSC Code:
12352100
PubChem Substance ID:
24894184
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.485 (lit.)

bp

138 °C/13 mmHg (lit.)

density

0.986 g/mL at 25 °C (lit.)

SMILES string

O=C(C1CCCCC1)C2CCCCC2

InChI

1S/C13H22O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2

InChI key

TWXWPPKDQOWNSX-UHFFFAOYSA-N

Related Categories

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6638
STBJ3374
STBG0691V
STBD9581V
S47056

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Matthew M D Roy et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 22(50), 18236-18246 (2016-11-01)
N-Heterocyclic carbene (NHC) complexes of Cd and Hg triflates (OTf) were prepared and their attempted conversion into rare cadmium and mercury hydrides was explored. In contrast to zinc, which forms stable [ZnH]+ complexes with NHCs, the heavier Cd and Hg
Christopher L Rock et al.
Dalton transactions (Cambridge, England : 2003), 48(2), 461-467 (2018-11-30)
The phosphine-substituted α-diimine Ni precursor, (Ph2PPrDI)Ni, has been found to catalyze alkene hydrosilylation in the presence of Ph2SiH2 with turnover frequencies of up to 124 h-1 at 25 °C (990 h-1 at 60 °C). Moreover, the selective hydrosilylation of allylic

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