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1,2-Epoxycyclododecane

Name: 1,2-Epoxycyclododecane
Brand: ALDRICH

(cis+trans), ≥95% (GC)

Synonym(s):

Cyclododecene oxide

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About This Item

Empirical Formula (Hill Notation):

C₁₂H₂₂O

CAS Number:

286-99-7

Molecular Weight:

182.30

EC Number:

206-012-4

UNSPSC Code:

12352100

PubChem Substance ID:

24857298

Beilstein/REAXYS Number:

106689

MDL number:

MFCD00005116

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Properties

assay

≥95% (GC)

refractive index

n20/D 1.481

bp

274-276 °C (lit.)

density

0.947 g/mL at 20 °C (lit.)

SMILES string

C1CCCCCC2OC2CCCC1

InChI

1S/C12H22O/c1-2-4-6-8-10-12-11(13-12)9-7-5-3-1/h11-12H,1-10H2

InChI key

VLJLXEKIAALSJE-UHFFFAOYSA-N

Description

General description

The kinetics of the rearrangement of 1,2-epoxycyclododecane, catalyzed by lithium bromide in the presence of polyethylene glycol 400, was studied.

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Investigating the therapeutic potential of herbal leads against drug resistant Listeria monocytogenes by computational virtual screening and in vitro assays.

Sinosh Skariyachan et al.

Journal of biomolecular structure & dynamics, 33(12), 2682-2694 (2015-01-07)

Listeria monocytogenes, a Gram-positive opportunistic food-borne pathogen, naturally resistant to many antibiotics and acquired resistance may be a concern in the nearer future. Hence, there is a scope for screening of novel therapeutic agents and drug targets, toward the treatment

Kinetics of the rearrangement of 1, 2-epoxycyclododecane and 1, 2-epoxycyclododeca-trans-5, 6- cis-9, 10-diene catalysed by lithium bromide in the presence of polyethylene glycol 400.

Filadska M and Balbolov E.

J. Mol. Catal., 73(2), 157-166 (1992)