所有图片(1)
About This Item
经验公式（希尔记法）:
C16H30N2Sn
CAS号:
分子量:
369.13
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
95%
表单
liquid
折射率
n20/D 1.512
密度
1.164 g/mL at 25 °C
SMILES字符串
CCCC[Sn](CCCC)(CCCC)c1ncccn1
InChI
1S/C4H3N2.3C4H9.Sn/c1-2-5-4-6-3-1;3*1-3-4-2;/h1-3H;3*1,3-4H2,2H3;
InChI key
WTFFOOAJSDVASL-UHFFFAOYSA-N
应用
2-(Tributylstannyl)pyrimidine is an organotin compound used in Stille coupling reaction. This can be used as one of the precursors in the synthesis of 2-aminopyridine oxazolidinones as potent and selective tankyrase (TNKS) inhibitors and the synthesis of canagliflozin, a novel inhibitor for sodium-dependent glucose cotransporter.
It can also be used in the preparation of various (2-pyrimidyl)silanes.
It can also be used in the preparation of various (2-pyrimidyl)silanes.
警示用语：
Danger
危险分类
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 1
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
The Stille Reaction
Farina V, et al.
Org. React. (1997)
C-Glucosides with heteroaryl thiophene as novel sodium-dependent glucose cotransporter 2 inhibitors.
Koga Y, et al.
Bioorganic & Medicinal Chemistry, 21(17), 5561-5572 (2013)
Structure-based design of 2-aminopyridine oxazolidinones as potent and selective tankyrase inhibitors.
Huang H, et al.
ACS Medicinal Chemistry Letters, 4(12), 1218-1223 (2013)
Catalytic Intermolecular Pauson? Khand-Type Reaction: Strong Directing Effect of Pyridylsilyl and Pyrimidylsilyl Groups and Isolation of Ru Complexes Relevant to Catalytic Reaction.
Itami K, et al.
Journal of the American Chemical Society, 126(35), 11058-11066 (2004)
Jesus Ivan Solares-Pascasio et al.
Molecules (Basel, Switzerland), 26(4) (2021-03-07)
Salvia amarissima Ortega was evaluated to determinate its antihyperglycemic and lipid profile properties. Petroleum ether extract of fresh aerial parts of S. amarissima (PEfAPSa) and a secondary fraction (F6Sa) were evaluated to determine their antihyperglycemic activity in streptozo-cin-induced diabetic (STID)
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