推荐产品
表单
solid
质量水平
反应适用性
reagent type: oxidant
mp
232 °C (dec.) (lit.)
官能团
amine
SMILES字符串
CN(C)C.O=S(=O)=O
InChI
1S/C3H9N.O3S/c2*1-4(2)3/h1-3H3;
InChI key
DXASQZJWWGZNSF-UHFFFAOYSA-N
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应用
用作硫酸化反应的反应物：
α-甲苯氧基酮合成中的亲核试剂
- 硫酸结合型白藜芦醇代谢产物的合成
- 用于抗 HIV-1 活性的壳寡糖
- 十二烷基硫代吡喃糖苷，作为表面活性剂用于对映体分离
- 促进依赖于硫酸化模式的信号通路活化的糖胺聚糖
- 多糖，如硫酸类肝素
α-甲苯氧基酮合成中的亲核试剂
相关产品
产品编号
说明
价格
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
Mikael Pedersen et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(4), 482-488 (2017-01-21)
After administration of steroids to animals the steroids are partially metabolised in the liver and kidney to phase 2 metabolites, i.e., glucuronic acid or sulphate conjugates. During analysis these conjugated metabolites are normally deconjugated enzymatically with aryl sulphatase and glucuronidase
Shuqian Hu et al.
Carbohydrate polymers, 236, 116052-116052 (2020-03-17)
In this study, a series water soluble sulfate polysaccharides (SPS) with different degrees of substitutions (DS = 0.02∼0.28) were prepared using a linear water-insoluble β-d-(1→3)-glucan. SPS-1, SPS-3 and SPS-7 with substitution degrees of 0.02, 0.06 and 0.25 were used as templates to
Jure Acimovic et al.
PloS one, 8(7), e68031-e68031 (2013-07-12)
24S- and 27-hydroxycholesterol (24OHC and 27OHC) are potent regulators of different biochemical systems in vitro and are the major circulating oxysterols. A small fraction of these oxysterols has been reported to be sulphated but there are no detailed studies. We
Juliane Strätz et al.
Macromolecular bioscience, 20(2), e1900403-e1900403 (2019-12-31)
Sulfated cellulose (CS) represents an interesting biopolymer due to bioactivity comparable to heparin. However, use of CS for making surface coatings or hydrogels requires the presence of reactive groups for covalent reactions. Here, an approach is presented to oxidize cellulose
Jianhong Yang et al.
Biopolymers, 103(10), 539-549 (2015-04-11)
The 6-amino-6-deoxychitosan (NC) and their 2, 6-di-N-sulfonated derivatives were prepared via N-phthaloylation, tosylation, azidation, hydrazinolysis, reduction of azide groups and N-sulfonation, and their structures were systematically characterized by FT-IR, 2D HSQC NMR, XRD, gel permeation chromatography (GPC), and elemental analysis.
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