跳转至内容
Merck
CN

318183

Sigma-Aldrich

硫酸甲酯 钠盐

别名:

甲基硫酸钠

登录查看公司和协议定价


About This Item

线性分子式:
CH3OSO3Na
CAS号:
分子量:
134.09
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

表单

powder

质量水平

杂质

<3% methanol
<5% water

mp

210 °C (lit.)

SMILES字符串

[Na+].COS([O-])(=O)=O

InChI

1S/CH4O4S.Na/c1-5-6(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1

InChI key

DZXBHDRHRFLQCJ-UHFFFAOYSA-M

应用

参与的反应物或试剂:
  • 微乳液法制备混杂纳米材料片层结构的研究
  • 离子液体辐射分解产生自由基离子的 EPR 研究
  • 微细胞研究特别是 1-苯甲酰基-1,2,4-三唑类化合物的水解缓速作用和混合胶束的自组装/微结构
硫酸甲酯钠盐可用于合成:
  • 基于硫酸甲酯阴离子的1,3,4-三烷基-1,2,3-三唑离子液体,用于Morita–Baylis–Hillman反应。
  • 与酚反应合成苯甲醚。
  • 羟基苯胺喹啉类化合物,用作RET激酶抑制剂。

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Synthesis of new triazolium-based ionic liquids and their use in the Morita-Baylis-Hillman reaction
F Alioune, et al.
Tetrahedron Letters, 56(36), 5128-5131 (2015)
Synthesis of anisole from phenol and sodium methyl sulfate, a byproduct from synthesis of medicine intermediates
Guoping W, et al.
Petrochemical Technology, 45(11), 1337-1337 (2016)
The discovery of substituted 4-(3-hydroxyanilino)-quinolines as potent RET kinase inhibitors
Robinett R G, et al.
Bioorganic & Medicinal Chemistry Letters, 17(21), 5886-5893 (2007)
Dean Kirson et al.
The Journal of pharmacology and experimental therapeutics, 364(1), 70-76 (2017-11-10)
The amino acid taurine is an endogenous ligand acting on glycine receptors (GlyRs), which is released by astrocytes in many brain regions, such as the nucleus accumbens and prefrontal cortex. Taurine is a partial agonist with an efficacy significantly lower
Jesús Oria-Hernández et al.
The Journal of biological chemistry, 280(45), 37924-37929 (2005-09-09)
For more than 50 years, it has been known that K(+) is an essential activator of pyruvate kinase (Kachmar, J. F., and Boyer, P. D. (1953) J. Biol. Chem. 200, 669-683). However, the role of K(+) in the catalysis by

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.

联系技术服务部门