68853
异喹啉
analytical standard
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关于此项目
经验公式（希尔记法）:
C9H7N
化学文摘社编号:
分子量:
129.16
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-341-8
Beilstein/REAXYS Number:
107549
MDL number:
InChI key
AWJUIBRHMBBTKR-UHFFFAOYSA-N
InChI
1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H
SMILES string
c1ccc2cnccc2c1
grade
analytical standard
assay
≥97.5% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.623 (lit.)
bp
242-243 °C (lit.)
mp
26-28 °C (lit.)
density
1.099 g/mL at 25 °C (lit.)
format
neat
storage temp.
2-8°C
Quality Level
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Application
有关合适的仪器技术的更多信息，请参阅产品的分析证书。想要获得更多支持，请联系技术服务部。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
Yusuke Ohta
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 130(7), 925-936 (2010-07-08)
A copper-catalyzed synthesis of 2-(aminomethyl)indole through domino three-component coupling-cyclization has been developed. This reaction proceeds through Mannich-type coupling of 2-ethynylanilines, aldehydes, and secondary amines, followed by hydroamination. This indole formation was applicable to the synthesis of 4-methylene-2,3,4,9-tetrahyro-1H-pyrido[3,4-b]indoles and 5,6,7,8-tetrahydrobenzo[e]indolo[2,3-c]azepines via
Beta-phenylethylamines and the isoquinoline alkaloids.
K W Bentley
Natural product reports, 18(2), 148-170 (2001-05-05)
Asymmetric synthesis of isoquinoline alkaloids.
Maria Chrzanowska et al.
Chemical reviews, 104(7), 3341-3370 (2004-07-15)
Kakali Bhadra et al.
Mini reviews in medicinal chemistry, 10(13), 1235-1247 (2010-08-19)
Alkaloids are a group of natural products with unmatched chemical diversity and biological relevance forming potential quality pools in drug screening. The molecular aspects of their interaction with many cellular macromolecules like DNA, RNA and proteins are being currently investigated
Fumihiko Sato et al.
Proceedings of the Japan Academy. Series B, Physical and biological sciences, 89(5), 165-182 (2013-05-15)
Plants produce a variety of secondary metabolites that possess strong physiological activities. Unfortunately, however, their production can suffer from a variety of serious problems, including low levels of productivity and heterogeneous quality, as well as difficulty in raw material supply.
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