推荐产品
质量水平
检测方案
98%
形式
liquid
折射率
n20/D 1.452 (lit.)
bp
84-85 °C/57 mmHg (lit.)
密度
0.909 g/mL at 25 °C (lit.)
SMILES字符串
CCC#CCO
InChI
1S/C5H8O/c1-2-3-4-5-6/h6H,2,5H2,1H3
InChI key
WLPYSOCRPHTIDZ-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
2-Pentyn-1-ol was employed as starting reagent for the synthesis of (-)-muricatacin. It was also used in the preparation of (2Z)-3-tributylstannyl-2-penten-1-ol.
警示用语：
Warning
危险分类
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
136.4 °F
闪点(°C)
58 °C
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
A Wada et al.
Chemical & pharmaceutical bulletin, 48(9), 1391-1394 (2000-09-19)
Palladium catalyzed cross coupling reactions of a vinyl triflate intermediate and various alkenyl stannanes afforded trisubstituted Z-olefins stereoselectively in high yields. These olefins were then converted to the corresponding 9Z-retinoic acids via Horner-Emmons reaction and subsequent basic hydrolysis in excellent
H Makabe et al.
Bioscience, biotechnology, and biochemistry, 57(6), 1028-1029 (1993-06-01)
The synthesis of (-)-muricatacin starting from 1-bromododecane and 2-pentyn-1-ol is described. 2-Pentadecyn-1-ol (4), which was prepared from 1-bromododecane (2) and 2-pentyn-1-ol (3), was converted to epoxy alcohol 6 through a two-step reaction sequence, 6 being successively submitted to tosylation, iodination
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