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Merck
CN

C94009

Sigma-Aldrich

4-氰基苯酚

95%

别名:

4-羟基苯甲腈

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关于此项目

线性分子式:
NCC6H4OH
CAS Number:
分子量:
119.12
Beilstein:
386130
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

95%

表单

crystals

mp

110-113 °C (lit.)

SMILES字符串

Oc1ccc(cc1)C#N

InChI

1S/C7H5NO/c8-5-6-1-3-7(9)4-2-6/h1-4,9H

InChI key

CVNOWLNNPYYEOH-UHFFFAOYSA-N

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应用

4-氰基苯酚是合成血管扩张剂左色满卡林的前体。4-氰基苯酚的溴化反应可生成溴苯腈,一种商业除草剂。它也可以用作低共熔溶剂(DES)混合物的组分。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Nitrogen-doped carbons prepared from eutectic mixtures as metal-free oxygen reduction catalysts.
Lopez-Salas N, et al.
Journal of Material Chemistry A, 4(2), 478-488 (2016)
N Higo et al.
Pharmaceutical research, 10(10), 1500-1506 (1993-10-01)
Attenuated total-reflectance infrared (ATR-IR) spectroscopy has been used to follow the penetration of a model compound (4-cyanophenol; CP) across human stratum corneum (SC) in vivo, in man. CP was administered for periods of 1, 2, or 3 hr, either (a)
F Pirot et al.
Proceedings of the National Academy of Sciences of the United States of America, 94(4), 1562-1567 (1997-02-18)
Attenuated-total-reflectance Fourier-transform-infrared spectroscopy has been used to rapidly and noninvasively quantify in vivo the uptake of a chemical into the outermost, and least permeable, layer of human skin (the stratum corneum). The objective of the experiment was to develop a
V H Mak et al.
Pharmaceutical research, 7(8), 835-841 (1990-08-01)
A novel application of attenuated total reflectance IR spectroscopy (ATR-IR) was used to monitor the outer several microns of the stratum corneum (SC) and, thereby, demonstrate enhanced percutaneous absorption in vivo in man. 4-Cyanophenol (CP) as a model permeant yielded
Synthesis and antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyrans.
Ashwood VA, et al.
Journal of Medicinal Chemistry, 29(11), 2194-2201 (1986)

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