212997
2-苯基-3-丁炔-2-醇
≥98%
别名:
α-Ethynyl-α-methylbenzenemethanol, 2-Hydroxy-2-phenyl-3-butyne, 2-Phenyl-2-hydroxy-3-butyne, 3-Hydroxy-3-phenyl-1-butyne, 3-Phenyl-1-butyn-3-ol, 3-Phenylbutyn-3-ol, Ethynylmethylphenylcarbinol, Methylphenylethynylcarbinol
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所有图片(3)
About This Item
线性分子式:
C6H5C(CH3)(OH)C≡CH
CAS号:
分子量:
146.19
Beilstein:
1100096
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
≥98%
表单
solid
沸点
102-103 °C/12 mmHg (lit.)
mp
47-49 °C (lit.)
官能团
hydroxyl
phenyl
SMILES字符串
CC(O)(C#C)c1ccccc1
InChI
1S/C10H10O/c1-3-10(2,11)9-7-5-4-6-8-9/h1,4-8,11H,2H3
InChI key
KSLSOBUAIFEGLT-UHFFFAOYSA-N
应用
用于含水、铜(II) 促进的与叠氮化合物的环加成反应，生成三唑类化合物。
Synlett, 957-957 (2006)
New 5-(2-ethenylsubstituted)-3 (2H)-furanones with in vitro antiproliferative activity.
Chimichi S, et al.
Tetrahedron, 59(28), 5215-5223 (2003)
Yanlong Gu et al.
The Journal of organic chemistry, 69(2), 391-394 (2004-01-17)
Reactions of propargylic alcohols with CO(2) in a [BMIm][PhSO(3)]/CuCl catalytic system to produce the corresponding alpha-methylene cyclic carbonates were conducted with high yields. Mild reaction conditions, enhanced rates, improved yields, and recyclable ionic liquid catalyst systems are the remarkable features
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