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Merck
CN

260789

8-氨基喹啉

98%

别名:

8-喹啉胺

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关于此项目

经验公式(希尔记法):
C9H8N2
化学文摘社编号:
分子量:
144.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-427-9
Beilstein/REAXYS Number:
114474
MDL number:
Assay:
98%
Form:
solid
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InChI key

WREVVZMUNPAPOV-UHFFFAOYSA-N

InChI

1S/C9H8N2/c10-8-5-1-3-7-4-2-6-11-9(7)8/h1-6H,10H2

SMILES string

Nc1cccc2cccnc12

assay

98%

form

solid

reaction suitability

reaction type: C-H Activation, reagent type: catalyst

bp

174 °C/26 mmHg (lit.)

Quality Level

mp

60-65 °C (lit.)

General description

8-氨基喹啉在低介电常数的介质中发出中等到微弱的荧光,但在强氢键或酸性水介质中不发出荧光 。研究了 8-氨基喹啉与铬 (Ⅲ)、锰 (Ⅱ)、铁 (Ⅱ) 和 (Ⅲ)、钴 (Ⅱ)、镍 (Ⅱ)、铜 (Ⅱ)、锌 (Ⅱ)、镉 (Ⅱ) 和铂 (Ⅱ) 盐的反应

Application

8-氨基喹啉已用于:
  • 制备锇碱基稳定的末端硼烯配合物
  • 分光光度法测定二价钯

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

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


历史批次信息供参考:

分析证书(COA)

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Rumei Cheng et al.
Analytical chemistry, 84(13), 5641-5644 (2012-06-05)
By incorporating the well-known fluorophore 8-aminoquinoline into graphene oxide, we have successfully prepared a turn-on fluorescent sensor capable of specific detection of D-glucosamine with a high selectivity and sensitivity. This methodology provides a new concept for the design and development
Spectrophotometric Determination of Palladium with 8-Aminoquinoline.
Gustin VK and Sweet TR.
Analytical Chemistry, 35(1), 44-46 (1963)
Kyalo Stephen Kanyiva et al.
Organic letters, 16(7), 1968-1971 (2014-03-22)
A palladium-catalyzed regioselective activation of C(sp(2))-H and C(sp(3))-H bonds of benzamides and carboxamides, followed by coupling with disilanes to afford organosilanes in moderate to high yields, with the aid of 8-aminoquinoline as a directing group, is reported. Catalytic C(sp(2))-H germanylation
Luis Carvalho et al.
Antimicrobial agents and chemotherapy, 55(9), 4204-4210 (2011-06-15)
The 8-aminoquinoline analogue sitamaquine (SQ) is an oral antileishmanial drug currently undergoing phase 2b clinical trials for the treatment of visceral leishmaniasis. In the present study, we investigated the mechanism of action of this drug in Leishmania donovani promastigotes. SQ
Some transition metal complexes of 8-aminoquinoline.
Fanning JC and Taylor LT.
J. Inorg. Nucl. Chem., 27(10), 2217-2223 (1965)

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