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Merck
모든 사진(2)

주요 문서

157872

Sigma-Aldrich

1,3-Dithiane

97%

동의어(들):

m-Dithiane (7CI), m-Dithiane (8CI)

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크기 선택

5 G
₩90,335
25 G
₩312,620

₩90,335


출고 가능일2025년 4월 16일세부사항


벌크 견적 요청

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보기 변경
5 G
₩90,335
25 G
₩312,620

About This Item

실험식(Hill 표기법):
C4H8S2
CAS Number:
Molecular Weight:
120.24
Beilstein:
102534
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

₩90,335


출고 가능일2025년 4월 16일세부사항


벌크 견적 요청

분석

97%

양식

solid

mp

52-54 °C (lit.)

작용기

thioether

SMILES string

C1CSCSC1

InChI

1S/C4H8S2/c1-2-5-4-6-3-1/h1-4H2

InChI key

WQADWIOXOXRPLN-UHFFFAOYSA-N

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관련 카테고리

일반 설명

1,3-Dithiane, a protected formaldehyde anion equivalent, serves as useful labeled synthon.[1]

애플리케이션

1,3-Dithiane was used as reagent for deoxygenation of sulfoxides to their corresponding sulfides.[2]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

194.0 °F - closed cup

Flash Point (°C)

90 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Al-Monsur Jiaul Haque et al.
Chemical communications (Cambridge, England), (32)(32), 4865-4867 (2009-08-05)
We report the use of 1,3-dithiane combined with aryldiazonium cation for the immobilization of biomolecules based on electrochemical addressing.
A I Noskov et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(1), 6-10 (2010-07-17)
The IR spectra of 1,3-dithiane-1-oxide (I) and 1,3-dithia-1-oxocyclohept-5-ene (II) were recorded in solution, solid and liquid phase over 4000-400 cm(-1) spectral range. It was found that both (I) and (II) in liquid phase and solutions exist in two conformations: (I)
Yuncong Chen et al.
Chemical communications (Cambridge, England), 48(42), 5094-5096 (2012-04-20)
A novel sensitive and specific Hg(2+) chemodosimeter, derived from 1',3'-dithiane-substituted 2,1,3-benzoxadiazole, displays "turn-on" fluorescent and colorimetric responses via an Hg(2+)-triggered aldehyde recovery reaction. Its potential to monitor Hg(2+) in living organisms has been demonstrated using zebrafish larvae.
Valerie J Peterson et al.
The Biochemical journal, 362(Pt 1), 173-181 (2002-02-07)
Apo and holo forms of retinoic acid receptors, and other nuclear receptors, display differential sensitivity to proteolytic digestion that likely reflects the distinct conformational states of the free and liganded forms of the receptor. We have developed a method for
Padmanabha V Kattamuri et al.
The Journal of organic chemistry, 76(8), 2792-2797 (2011-03-17)
A series of α-amino-1,3-dithianes have been synthesized via the asymmetric Umpolung reaction of 2-lithio-1,3-dithianes with chiral N-phosphonyl imines in good chemical yields (up to 82%) and good to excellent diastereoselectivities (>99:1). The manner by which chiral N-phosphonyl imines are slowly

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