Q2125
2-甲基喹啉
analytical standard, ≥90% (GC)
别名:
喹哪啶
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关于此项目
经验公式（希尔记法）:
C10H9N
化学文摘社编号:
分子量:
143.19
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-085-1
Beilstein/REAXYS Number:
110309
MDL number:
产品名称
2-甲基喹啉, analytical standard, ≥90% (GC)
InChI key
SMUQFGGVLNAIOZ-UHFFFAOYSA-N
InChI
1S/C10H9N/c1-8-6-7-9-4-2-3-5-10(9)11-8/h2-7H,1H3
SMILES string
Cc1ccc2ccccc2n1
grade
analytical standard
assay
≥90% (GC)
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
refractive index
n20/D 1.612 (lit.)
bp
105-107 °C/10 mmHg (lit.)
248 °C (lit.)
mp
−9-−3 °C (lit.)
density
1.058 g/mL at 25 °C (lit.)
application(s)
forensics and toxicology
pharmaceutical (small molecule)
format
neat
Quality Level
Gene Information
human ... CYP1A2(1544)
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
D Ferri et al.
Journal of the American Chemical Society, 123(48), 12074-12084 (2001-11-29)
An in situ attenuated total reflection study of the chiral solid-liquid interface created by cinchonidine adsorption on a Pt/Al(2)O(3) model catalyst is presented. Experiments were performed in the presence of dissolved hydrogen, that is under conditions used for the heterogeneous
J Ortuño et al.
Fish & shellfish immunology, 12(1), 49-59 (2002-02-28)
Anaesthesia may depress the immune system in mammals, but there is no available information on this topic in fish. In the present work, four anaesthetics that are used in aquaculture, MS222 (0 19 mM), benzocaine (0.21 mM), 2-phenoxyethanol (16 mM)
Robert M Gengan et al.
Molecules (Basel, Switzerland), 15(5), 3171-3178 (2010-07-27)
An efficient synthesis of a methyl derivative of the indoloquinoline alkaloid cryptosanguinolentine based on microwave-assisted reactions is described. The microwave-assisted synthesis of an intermediate 4-hydroxy-2-methylquinoline yielded 86% of the desired product and other intermediates prepared yielded high % of products
Alan R Katritzky et al.
The Journal of organic chemistry, 75(11), 3938-3940 (2010-05-13)
2-Methyl- and 4-methylpyridine and 2-methylquinoline are converted by benzotriazole-activated (Cbz)-protected amino acids into chiral potential novel pharmacophore aminoacyl conjugates (33-53%).
Massimo La Deda et al.
Dalton transactions (Cambridge, England : 2003), (2)(2), 330-339 (2005-12-21)
This paper reports the synthesis, characterisation and photophysical investigation of the homologous series of blue-emitting pentacoordinated AlQ'(2)L complexes 1-6, where Q' is 2-methylquinolin-8-olate and L is a phenolate substituted in para to the oxygen donor atom. Both electron attracting and
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