196274
硫代吗啉
98%
别名:
四氢-2H-1,4-噻嗪, 巯基吗啉
登录 查看组织和合同定价。
选择尺寸
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-660-2
Beilstein/REAXYS Number:
102550
MDL number:
Assay:
98%
InChI key
BRNULMACUQOKMR-UHFFFAOYSA-N
InChI
1S/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2
SMILES string
C1CSCCN1
assay
98%
refractive index
n20/D 1.538 (lit.)
bp
169 °C (lit.)
solubility
organic solvents: miscible(lit.), water: miscible(lit.)
density
1.026 g/mL at 25 °C (lit.)
functional group
thioether
Quality Level
General description
硫代吗啉与 Cu (II)、Pt (II) 和 Ni (II) 盐反应生成复合物，并对其催化活性进行了研究 。
Application
硫代吗啉已经被用于制备：
- N-Boc-α-烷基-β-（ 仲-氨基）丙氨酸
- 硫代吗啉- N -硼烷
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
145.4 °F - closed cup
flash_point_c
63 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Synthesis and comparative reactivity of thiomorpholine-borane: aqueous hydrolysis and oxidation by hypochlorite.
Amezcua CA, et al.
Inorgorganica Chimica Acta, 290(1), 80-85 (1999)
Mesut Kacan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 118, 572-577 (2013-10-05)
Several Cu(II), Pt(II) and Ni(II) complexes of N-substituted, piperazine (NN donor), morpholine (NO donor) and thiomorpholine (NS donor) derivatives were synthesized and their thermal behavior and catalytic activity in epoxidation reaction of cis-diphenylethylene were studied using oxygen sources NaOCl. The
Saurav Bera et al.
ACS combinatorial science, 14(1), 1-4 (2011-12-01)
Diastereoselective trans-2,5-disubstituted amino acids derived diverse morpholines, piperazines and thiomorpholines were prepared in 30 min-1 h with high yields through iodine-mediated 6-exotrig type cyclization from a single common synthetic intermediate. The displacement of iodine with hydride ion gave a methyl
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.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持