H31859
5-羟基苯并吡咯
97%
别名:
5-羟基吲哚, 5-羟基苯并吡咯, NSC 87503
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关于此项目
经验公式（希尔记法）:
C8H7NO
化学文摘社编号:
分子量:
133.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-782-6
Beilstein/REAXYS Number:
112349
MDL number:
Assay:
97%
产品名称
5-羟基苯并吡咯, 97%
InChI key
LMIQERWZRIFWNZ-UHFFFAOYSA-N
InChI
1S/C8H7NO/c10-7-1-2-8-6(5-7)3-4-9-8/h1-5,9-10H
SMILES string
Oc1ccc2[nH]ccc2c1
assay
97%
mp
106-108 °C (lit.)
Quality Level
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Application
- 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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
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)
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
Eva-Maria Karg et al.
Journal of medicinal chemistry, 52(11), 3474-3483 (2009-06-06)
Pharmacological suppression of leukotriene biosynthesis by inhibitors of 5-lipoxygenase (5-LO) is a strategy to intervene with inflammatory and allergic disorders. We recently presented 2-amino-5-hydroxy-1H-indoles as efficient 5-LO inhibitors in cell-based and cell-free assays. Structural optimization led to novel benzo[g]indole-3-carboxylates exemplified
Ruth Livingstone et al.
The Journal of chemical physics, 135(19), 194307-194307 (2011-11-25)
Time-resolved photoelectron spectroscopy was used to obtain new information about the dynamics of electronic relaxation in gas-phase indole and 5-hydroxyindole following UV excitation with femtosecond laser pulses centred at 249 nm and 273 nm. Our analysis of the data was
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