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品質等級
化驗
98%
折射率
n20/D 1.538 (lit.)
bp
169 °C (lit.)
溶解度
organic solvents: miscible(lit.)
water: miscible(lit.)
密度
1.026 g/mL at 25 °C (lit.)
官能基
thioether
SMILES 字串
C1CSCCN1
InChI
1S/C4H9NS/c1-3-6-4-2-5-1/h5H,1-4H2
InChI 密鑰
BRNULMACUQOKMR-UHFFFAOYSA-N
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一般說明
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 。
應用
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
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
145.4 °F - closed cup
閃點(°C)
63 °C - closed cup
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
其他客户在看
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
Synthesis and comparative reactivity of thiomorpholine-borane: aqueous hydrolysis and oxidation by hypochlorite.
Inorgorganica Chimica Acta, 290(1), 80-85 (1999)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(12), 2737-2757 (2002-10-25)
The natural abundance 15N-NMR chemical shifts of selected aliphatic amines, 2-substituted pyridine type compounds, bialicyclic tertiary amines have been measured as a function of the nature of the solvent. In the case of cyclic aliphatic amines, like piperidine, morpholine, piperazine
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
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
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