467979
1,3-Dithiolane
97%
Sinônimo(s):
1,3-Dithiacyclopentane
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About This Item
Produtos recomendados
Ensaio
97%
índice de refração
n20/D 1.599 (lit.)
pb
183 °C (lit.)
densidade
1.235 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
C1CSCS1
InChI
1S/C3H6S2/c1-2-5-3-4-1/h1-3H2
chave InChI
IMLSAISZLJGWPP-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
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.
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
154.4 °F - closed cup
Ponto de fulgor (°C)
68 °C - closed cup
Certificados de análise (COA)
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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.
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
Differentiation between carbonyls and acetals in 1, 3-dithiane and 1, 3-dithiolane synthesis catalyzed by organotin triflates.
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.
Org. Mass Spectrom., 6(4), 415-423 (1972)
Elemental fluorine. Part 5. Reactions of 1, 3-dithiolanes and thioglycosides with fluorine-iodine mixtures.
Journal of the Chemical Society. Perkin Transactions 1, 16, 1941-1944 (1996)
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