Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

458597

Sigma-Aldrich

Cyclohexanone dimethyl ketal

99%

Synonym(s):

1,1-Dimethoxycyclohexane

Sign Into View Organizational & Contract Pricing

Select a Size

50 ML
$92.30

$92.30

Estimated to ship onMarch 31, 2025

Request a Bulk Order
All Photos(1)

Select a Size

Change View
50 ML
$92.30

About This Item

Linear Formula:
C6H10(OCH3)2
CAS Number:
933-40-4
Molecular Weight:
144.21
MDL number:
MFCD00043714
UNSPSC Code:
12352100
PubChem Substance ID:
24869484
NACRES:
NA.22
assay:
99%

$92.30

Estimated to ship onMarch 31, 2025

Request a Bulk Order

Quality Level

100

assay

99%

refractive index

n20/D 1.439 (lit.)

bp

83 °C/50 mmHg (lit.)

density

0.948 g/mL at 25 °C (lit.)

functional group

ether
ketal

SMILES string

COC1(CCCCC1)OC

InChI

1S/C8H16O2/c1-9-8(10-2)6-4-3-5-7-8/h3-7H2,1-2H3

InChI key

XPIJMQVLTXAGME-UHFFFAOYSA-N

General description

Cyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether.[1] It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or homopropargylic alcohol, respectively.[2]

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

111.2 °F - closed cup

flash_point_c

44 °C - closed cup

ppe

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCC3043
MKBW2528V
MKBN6156V
MKBJ0279V
MKBC3886V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Ogata et al.
Journal of medicinal chemistry, 30(6), 1054-1068 (1987-06-01)
To find orally active antifungal agents, novel imidazolyl- and 1,2,4-triazolylpropanolones I and related compounds II-IV were synthesized. Compounds I were derived from ketones V (method A), alpha-diketone IX (method B), alpha-hydroxy ketones X (method C), alpha-chloro ketone XII (method D)
Preparation of ketone acetals from linear ketones and alcohols.
Lorette NB, et al.
The Journal of Organic Chemistry, 24(11), 1731-1733 (1959)
Trimethysilyl triflate in organic synthesis
Noyori R, et al.
Tetrahedron, 37(23, 3899-3910 (1981)
Indium mediated allylation and propargylation reactions of dimethyl acetals and ketals.
Kwon JS, et al.
Tetrahedron Letters, 42(10), 1957-1959 (2001)
Sebastian Krickl et al.
Physical chemistry chemical physics : PCCP, 19(35), 23773-23780 (2017-07-01)
In this contribution, we (i) link the mesoscopic structuring of the binary structured solvent mixture H

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service