Merck
CN

520039

Sigma-Aldrich

2-乙炔苯甲醇

95%

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线性分子式:
HC≡CC6H4CH2OH
CAS号:
分子量:
132.16
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

检测方案

95%

形式

solid

mp

66-70 °C (lit.)

SMILES string

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

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519235667706686336
2-Ethynylbenzyl alcohol 95%

Sigma-Aldrich

520039

2-乙炔苯甲醇

4-Ethynylbenzyl alcohol 97%

Sigma-Aldrich

519235

4-乙炔苯甲醇

2-(Bromomethyl)benzyl alcohol 95%

Sigma-Aldrich

667706

2-(溴甲基)苄醇

form

solid

form

-

form

solid

form

liquid

mp

66-70 °C (lit.)

mp

40-44 °C (lit.)

mp

66-68 °C

mp

-

象形图

Exclamation markHealth hazard

警示用语:

Danger

危险声明

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)
Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride.
Hiroya K, et al.
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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.
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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
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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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Functionalized Alkynes

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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