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Merck
CN

519235

4-乙炔苯甲醇

97%

别名:

4-羟甲基苯乙炔

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关于此项目

线性分子式:
HC≡CC6H4CH2OH
化学文摘社编号:
分子量:
132.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

4-乙炔苯甲醇, 97%

Quality Level

InChI

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

SMILES string

OCc1ccc(cc1)C#C

InChI key

QCZORVSTESPHCO-UHFFFAOYSA-N

assay

97%

mp

40-44 °C (lit.)

functional group

hydroxyl

Application

  • 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。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
A fluorogenic `click?reaction of azidoanthracene derivatives.
Xie F, et al.
Tetrahedron, 64(13), 2906-2914 (2008)
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
Kideog Bae et al.
Analytical chemistry, 92(1), 740-748 (2019-11-22)
The dynamics of mitochondria in live cells play a pivotal role in biological events such as cell metabolism, early stage apoptosis, and cell differentiation. Triphenylphosphonium (TPP) is a commonly used mitochondria-targeting agent for mitochondrial studies. However, there has been a
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)

商品

Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.

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