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196274

硫代吗啉

Name: 硫代吗啉
Brand: ALDRICH

98%

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:

123-90-0

分子量:

103.19

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851748

EC Number:

204-660-2

Beilstein/REAXYS Number:

102550

MDL number:

MFCD00005974

Assay:

98%

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属性

Quality Level

100

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

SMILES string

C1CSCCN1

InChI

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

InChI key

BRNULMACUQOKMR-UHFFFAOYSA-N

说明

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

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P301 + P330 + P331 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 + P310 - P501

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Complexation, thermal and catalytic studies of N-substituted piperazine, morpholine and thiomorpholine with some metal ions.

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

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)

One-pot multicomponent synthesis of two novel thiolactone scaffolds.

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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全球贸易项目编号

货号	GTIN
196274-25G	04061838118493
196274-5G	04061838761996