Merck
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文件

520039

Sigma-Aldrich

2-乙炔苯甲醇

95%

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线性分子式:
HC≡CC6H4CH2OH
CAS号:
10602-08-1
分子量:
132.16
MDL编号:
MFCD06200681
PubChem化学物质编号:
24874088
NACRES:
NA.22

检测方案

95%

形式

solid

mp

66-70 °C (lit.)

SMILES字符串

OCc1ccccc1C#C

InChI

1S/C9H8O/c1-2-8-5-3-4-6-9(8)7-10/h1,3-6,10H,7H2

InChI key

ZKCWIJQOZHADEM-UHFFFAOYSA-N

象形图

Exclamation markHealth hazard
GHS07,GHS08

警示用语：

Danger

危险声明

H302 - H319 - H334

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 2

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Preparation, Structural and Spectral Properties of Poly (2-ethynylbenzyl alcohol).
Lee WC, et al.
Mol. Cryst. Liq. Cryst., 513(1), 196-204 (2009)
Synthesis of 1-(Alkoxycarbonyl) methylene-1, 3-dihydroisobenzofurans and 4-(Alkoxycarbonyl) benzo [c] pyrans by Palladium-Catalysed Oxidative Carbonylation of 2-Alkynylbenzyl Alcohols, 2-Alkynylbenzaldehydes and 2-Alkynylphenyl Ketones.
Bacchi A, et al.
European Journal of Organic Chemistry, 3, 574-585 (2004)
Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride.
Hiroya K, et al.
Tetrahedron, 57(48), 9697-9710 (2001)
Xueqing Wang et al.
The Journal of organic chemistry, 63(21), 7357-7363 (2001-10-24)
An attempt to trap radical intermediates during the monoamine oxidase (MAO) catalyzed oxidation of amines by intramolecular cyclization with an activated alkene that is built into the substrate was unsuccessful. (E)-2-(Iodoethenyl)benzylamine (3a) was shown to be a reversible inhibitor of
Subhasish Tapadar et al.
Bioorganic & medicinal chemistry, 23(24), 7543-7564 (2015-11-21)
Inhibition of the enzymatic activity of histone deacetylase (HDAC) is a promising therapeutic strategy for cancer treatment and several distinct small molecule histone deacetylase inhibitors (HDACi) have been reported. We have previously identified a new class of non-peptide macrocyclic HDACi
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Alkynes contain a highly versatile functional group that may be utilized for numerous reactions such as electrophilic additions of hydrogen, halogens, hydrogen halides, or water; metathesis; hydroboration; oxidative cleavage; C–C coupling; and cycloadditions

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