所有图片(1)

文件

H31859

5-羟基苯并吡咯

Name: 5-羟基苯并吡咯
Brand: ALDRICH

97%

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所有图片(1)

别名:

5-羟基吲哚, 5-羟基苯并吡咯, NSC 87503

经验公式（希尔记法）:

C₈H₇NO

CAS号:

1953-54-4

分子量:

133.15

Beilstein:

112349

EC 号:

217-782-6

MDL编号:

MFCD00005677

PubChem化学物质编号:

24895561

NACRES:

NA.22

检测方案

97%

mp

106-108 °C (lit.)

SMILES string

Oc1ccc2[nH]ccc2c1

InChI

1S/C8H7NO/c10-7-1-2-8-6(5-7)3-4-9-8/h1-5,9-10H

InChI key

LMIQERWZRIFWNZ-UHFFFAOYSA-N

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应用

用于制备抗肿瘤剂（氧咪唑烷基/氧嘧啶基）苯磺酸酯和微管蛋白抑制剂的反应物
用于制备邻氨基苯甲酸的反应物
用于制备吲哚化合物作为多巴胺D2受体拮抗剂的反应物
用于制备含萘酰亚胺或咔唑的人β-肾上腺素受体配体的反应物
用于制备天然辐射防护剂黑色素的反应物
用于制备 PKCθ 抑制剂5-乙烯基-3-吡啶腈的反应物

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Simultaneous determination of 5-hydroxyindoles and catechols from urine using polymer monolith microextraction coupled to high-performance liquid chromatography with fluorescence detection.

Yu-Bo Wu et al.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 877(20-21), 1847-1855 (2009-06-02)

To make analytes amenable for fluorescence (FL) detection, polymer monolith microextraction (PMME) coupled to high-performance liquid chromatography with FL detection was developed for the simultaneous determination of catechols and 5-hydroxyindoleamines (5-HIAs) from urine samples. In this method, a two-step pre-column

Synthesis and structure based optimization of 2-(4-phenoxybenzoyl)-5-hydroxyindole as a novel CaMKII inhibitor.

Masafumi Komiya et al.

Bioorganic & medicinal chemistry, 20(23), 6840-6847 (2012-10-24)

Based on 2-(4-phenoxybenzoyl)-5-hydroxyindole (2), a novel structural class of CaMKII inhibitors were synthesized and further optimized. The strong acidity of the hydroxyl group and the lipophilic group at the 4 and 6-positions were found to be necessary for strong CaMKII

Ribosomal synthesis of cyclic peptides with a fluorogenic oxidative coupling reaction.

Yusuke Yamagishi et al.

Chembiochem : a European journal of chemical biology, 10(9), 1469-1472 (2009-05-28)

Electronic structure of 5-hydroxyindole: from gas phase to explicit solvation.

David Robinson et al.

The journal of physical chemistry. B, 113(8), 2535-2541 (2009-02-07)

We have investigated the absorption and emission spectrum of 5-hydroxyindole in the gas phase and in various solvents. 5-Hydroxyindole is the fluorophore of the non-natural amino acid 5-hydroxytryptophan, which has attracted recent interest as a novel intrinsic probe for protein

Simultaneous analysis of 29 synthetic cannabinoids and metabolites, amphetamines, and cannabinoids in human whole blood by liquid chromatography-tandem mass spectrometry - A New Zealand perspective of use in 2018.

Rui Shen Ong et al.

Drug testing and analysis, 12(2), 195-214 (2019-10-09)

We describe the validation of a method for the simultaneous analysis of 29 synthetic cannabinoids (SCs) and metabolites, 4 amphetamines, and 2 cannabinoids in human whole blood. This method enables one analysis to cover what previously required multiple analyses for

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