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Merck
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467979

Sigma-Aldrich

1,3-Dithiolane

97%

동의어(들):

1,3-Dithiacyclopentane

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크기 선택

5 G
₩171,028

₩171,028

구입 가능 여부는 고객센터에 문의하십시오.
벌크 견적 요청
모든 사진(1)

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5 G
₩171,028

About This Item

실험식(Hill 표기법):
C3H6S2
CAS Number:
4829-04-3
Molecular Weight:
106.21
MDL number:
MFCD00041425
UNSPSC 코드:
12352100
PubChem Substance ID:
24870452
NACRES:
NA.22

₩171,028

구입 가능 여부는 고객센터에 문의하십시오.
벌크 견적 요청

Quality Level

100

분석

97%

refractive index

n20/D 1.599 (lit.)

bp

183 °C (lit.)

density

1.235 g/mL at 25 °C (lit.)

작용기

thioether

SMILES string

C1CSCS1

InChI

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

InChI key

IMLSAISZLJGWPP-UHFFFAOYSA-N

관련 카테고리

일반 설명

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

154.4 °F - closed cup

Flash Point (°C)

68 °C - closed cup

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
MKCN9627
MKBZ6619V
MKBG8561
06614TC
04709LB

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문서 라이브러리 방문

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.
Alexandra Papanikos et al.
Journal of combinatorial chemistry, 6(2), 181-195 (2004-03-09)
A synthetic strategy for the formation of resin-bound internal alpha-keto amide peptides suitable for protease inhibitor screening on solid support is presented. This general approach is based on the incorporation of alpha-keto amide building blocks during solid-phase peptide synthesis (SPPS).
Kalevi Pihlaja et al.
Magnetic resonance in chemistry : MRC, 49(7), 443-449 (2011-05-07)
1-Oxo-1,3-dithiolane (4) and its cis- and trans-2-methyl (5,6), -4-methyl (7,8) and -5-methyl (9,10) derivatives were prepared by oxidizing the corresponding 1,3-dithiolanes (1-3) with NaIO(4) in water. The oxides were purified and their isomers separated using thin layer chromatography. The structural
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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