质量水平
检测方案
98%
形式
liquid
旋光性
[α]20/D −18°, c = 2.4 in methanol
折射率
n20/D 1.45 (lit.)
bp
181 °C (lit.)
密度
1.097 g/mL at 25 °C (lit.)
SMILES字符串
O[C@@H]1CCOC1
InChI
1S/C4H8O2/c5-4-1-2-6-3-4/h4-5H,1-3H2/t4-/m1/s1
InChI key
XDPCNPCKDGQBAN-SCSAIBSYSA-N
应用
(R)-(-)-3-Hydroxytetrahydrofuran may be used as building block in the synthesis of potent HIV protease inhibitors.
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
179.6 °F
闪点(°C)
82 °C
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Diethyl zinc catalyzed diastereoselective addition of ketenes to (S)-(+)-3-hydroxytetrahydrofuran.
Tetrahedron Letters, 42(34), 5985-5987 (2001)
Angle-Resolved Photoelectron Spectroscopy of Randomly Oriented 3-Hydroxytetrahydrofuran Enantiomers.
ChemPhysChem, 6(6), 1164-1168 (2005)
Journal of labelled compounds & radiopharmaceuticals, 57(12), 687-694 (2014-10-22)
Empagliflozin, (2S,3R,4R,5S,6R)-2-[4-chloro-3-[[4-[(3S)-oxolan-3-yl]oxyphenyl]methyl]phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol was recently approved by the FDA for the treatment of chronic type 2 diabetes mellitus. Herein, we report the synthesis of carbon-13 and carbon-14 labeled empagliflozin. Carbon-13 labeled empagliflozin was prepared in five steps and in 34% overall
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