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467979

Sigma-Aldrich

1,3-Dithiolane

97%

Synonym(s):

1,3-Dithiacyclopentane

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About This Item

Empirical Formula (Hill Notation):
C3H6S2
CAS Number:
Molecular Weight:
106.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.599 (lit.)

bp

183 °C (lit.)

density

1.235 g/mL at 25 °C (lit.)

functional group

thioether

SMILES string

C1CSCS1

InChI

1S/C3H6S2/c1-2-5-3-4-1/h1-3H2

InChI key

IMLSAISZLJGWPP-UHFFFAOYSA-N

General description

1,3-Dithiolane ,a sulfur containing heterocyclic building block, is a cyclic thioether. Fragmentation modes of 1,3-oxathiolane under electron-impact have been investigated.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

154.4 °F - closed cup

Flash Point(C)

68 °C - closed cup


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Differentiation between carbonyls and acetals in 1, 3-dithiane and 1, 3-dithiolane synthesis catalyzed by organotin triflates.
Sato T, et al.
The Journal of Organic Chemistry, 58(18), 4971-4978 (1993)
Ionization and dissociation of cyclic ethers and thioethers by electron-impact. A comparison between 1, 3-dioxolane, 1, 3-dithiolane and 1, 3-oxathiolane.
Conde-Caprace G and Collin JE.
Org. Mass Spectrom., 6(4), 415-423 (1972)
Elemental fluorine. Part 5. Reactions of 1, 3-dithiolanes and thioglycosides with fluorine-iodine mixtures.
Chambers RD, et al.
Journal of the Chemical Society. Perkin Transactions 1, 16, 1941-1944 (1996)
I M Hussaini et al.
Acta pharmacologica Sinica, 21(10), 897-904 (2001-08-15)
To investigate the effect of a group of novel synthetic dithiolane analogs of lignans and a well characterized platelet-activating factor (PAF) receptor antagonist, L659,989 on PAF-receptor binding, IFN-gamma- and lipopolysaccharide (LPS)-induced NO production, and steady-state inducible nitric-oxide synthase (iNOS) mRNA
Sylvie Goncalves et al.
Chemical communications (Cambridge, England), 46(31), 5778-5780 (2010-07-06)
A concise and diastereoselective formal total synthesis of triptolide, a natural product with a wide range of biological properties, is described. The key reaction is an unprecedented 6-endo-Trig cationic cyclization of a 2-alkenyl-1,3-dithiolane precursor induced by TMSOTf as Lewis acid.

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