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Merck
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文件

467979

Sigma-Aldrich

1,3-二硫代坊

97%

别名:

1,3-Dithiacyclopentane

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About This Item

经验公式（希尔记法）:
C3H6S2
CAS号:
4829-04-3
分子量:
106.21
MDL號碼:
MFCD00041425
分類程式碼代碼:
12352100
PubChem物質ID:
24870452
NACRES:
NA.22

化驗

97%

折射率

n20/D 1.599 (lit.)

bp

183 °C (lit.)

密度

1.235 g/mL at 25 °C (lit.)

SMILES 字串

C1CSCS1

InChI

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

InChI 密鑰

IMLSAISZLJGWPP-UHFFFAOYSA-N

相关类别

一般說明

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.

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

154.4 °F - closed cup

閃點（°C）

68 °C - closed cup

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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.
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)
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