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Merck
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文件

519235

Sigma-Aldrich

4-乙炔苯甲醇

97%

别名:

4-羟甲基苯乙炔

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About This Item

线性分子式:
HC≡CC6H4CH2OH
CAS号:
10602-04-7
分子量:
132.16
MDL號碼:
MFCD05664205
分類程式碼代碼:
12352100
PubChem物質ID:
24874070
NACRES:
NA.22

化驗

97%

mp

40-44 °C (lit.)

SMILES 字串

OCc1ccc(cc1)C#C

InChI

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

InChI 密鑰

QCZORVSTESPHCO-UHFFFAOYSA-N

相关类别

應用

  • 4-乙炔基苯甲醇可用于铂-乙炔树枝状大分子轮烷和芳基乙炔的合成。
  • 用于制备芳基烷基标签糖，帮助含半胱氨酸肽的光诱导糖基化。
  • 它也可以作为前体，通过 Cu (I) 催化的叠氮-炔环加成 (CuAAC) 链接反应合成荧光探针。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H302,H319

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 2

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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Palladium/silver-cocatalyzed tandem reactions of oxabenzonorbornadienes with substituted arylacetylenes: A simple method for the preparation of 1, 2-diarylethanones and 1, 2-diarylacetylenes.
Chen J, et al.
Organometallics, 34(17), 4318-4322 (2015)
Synthesis and Optical Properties of a Polyacetylene with Hydroxy Funtional Groups: Poly (4-ethynylbenzyl Alcohol).
Gal YS, et al.
Mol. Cryst. Liq. Cryst., 601(1), 151-158 (2014)
Susimaire P Mantoani et al.
Molecules (Basel, Switzerland), 21(2), doi:10-doi:10 (2016-02-11)
Alzheimer's disease (AD) is the most prevalent neurodegenerative disorder worldwide. Currently, the only strategy for palliative treatment of AD is to inhibit acetylcholinesterase (AChE) in order to increase the concentration of acetylcholine in the synaptic cleft. Evidence indicates that AChE
A fluorogenic `click?reaction of azidoanthracene derivatives.
Xie F, et al.
Tetrahedron, 64(13), 2906-2914 (2008)
Synthesis and conformation effects of poly (phenylacetylene) s having chiral and racemic polylactide pendants.
Zhang C, et al.
Polymer International, 61(7), 1158-1162 (2012)
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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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