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Merck
CN

88885

Sigma-Aldrich

硫代吗啉

purum, ≥97.0% (GC)

别名:

四氢-2H-1,4-噻嗪, 巯基吗啉

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关于此项目

经验公式(希尔记法):
C4H9NS
化学文摘社编号:
分子量:
103.19
Beilstein:
102550
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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等级

purum

方案

≥97.0% (GC)

折射率

n20/D 1.538 (lit.)
n20/D 1.540

沸点

169 °C (lit.)

密度

1.026 g/mL at 25 °C (lit.)

SMILES字符串

C1CSCCN1

InChI

1S/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2

InChI key

BRNULMACUQOKMR-UHFFFAOYSA-N

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象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

145.4 °F - closed cup

闪点(°C)

63 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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[Study of antiradiation drugs. I. Synthesis of some mercapto and amino derivatives of thiomorpholine (author's transl)].
F X Chen et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 15(8), 482-488 (1980-08-01)
Upinder Singh et al.
Bioorganic & medicinal chemistry letters, 13(23), 4209-4212 (2003-11-19)
Combinatorial libraries of N-acylated 5-(S)-aminomethyloxazolidinone derivatives of S-oxide and S,S-dioxide tetrahydro-4(2H)-thiopyranyl and thiomorpholine phenyloxazolidinone series have been synthesized on a solid phase and evaluated for antimicrobial activity. Several novel potent leads have been identified, including orally active oxazolidinones with enhanced
An annulation reaction for the synthesis of morpholines, thiomorpholines, and piperazines from beta-heteroatom amino compounds and vinyl sulfonium salts.
Muhammad Yar et al.
Angewandte Chemie (International ed. in English), 47(20), 3784-3786 (2008-04-12)
Amany Belal
Bioorganic chemistry, 59, 124-129 (2015-03-10)
A new series of pyrrolizine derivatives 4-8c were synthesized, their structures were confirmed by spectral and elemental analyses. Cytotoxic activity of these compounds was evaluated against breast (MCF7), colon (HCT116) and liver (HEPG2) cancer cell lines using sulphorhodamine-B (SRB) assay
B Beck et al.
Molecular diversity, 14(3), 479-491 (2010-04-22)
We designed two novel thiolactone scaffolds. Both scaffolds can be accessed by a convergent Ugi multicomponent reaction (MCR) and are, thus, amenable to library synthesis. Design, stereoselectivity, structures, full experimental details, and virtual libraries will be reported.

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