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质量水平
方案
99%
表单
crystals
沸点
266-267 °C (lit.)
mp
34-37 °C (lit.)
密度
1.23 g/mL at 25 °C (lit.)
SMILES字符串
Clc1ccc2ccccc2n1
InChI
1S/C9H6ClN/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H
InChI key
OFUFXTHGZWIDDB-UHFFFAOYSA-N
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危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
230.0 °F - closed cup
闪点(°C)
110 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
从最新的版本中选择一种：
分析证书(COA)
Lot/Batch Number
K Shiva Kumar et al.
Bioorganic & medicinal chemistry, 20(7), 2199-2207 (2012-03-06)
A number of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives were synthesized via AlCl(3)-mediated C-C bond forming reaction between 2-chloroquinoline-3-carbonitrile and various indoles. The methodology does not require any N-protection of the indoles employed and provided the corresponding products in good yields. The molecular structure
S Fetzner et al.
FEMS microbiology letters, 112(2), 151-157 (1993-09-01)
Resting cells of Pseudomonas putida strain 86 were grown on quinoline transformed 2-chloroquinoline to 2-chloro-cis-7,8-dihydro-7,8-dihydroxyquinoline which was not converted further. 7,8-Dioxygenating activity was present when the enzymes of quinoline catabolism were induced. Quinoline-grown cells of strain 86 treated simultaneously with
Yubin Ji et al.
Biomedical chromatography : BMC, 34(8), e4845-e4845 (2020-04-09)
An ultra-high performance liquid chromatography tandem mass spectrometry method was developed for determination of homocysteine (HCY) in human plasma. The HCY was derivatized with 2-chloro-1-methylquinolinium tetrafluoroborate and isolated using solid-phase extraction. Derivatization, isolation and detection procedures were optimized. Satisfactory linearity
Amol A Nagargoje et al.
Chemistry & biodiversity, 17(2), e1900624-e1900624 (2019-12-22)
In search for new fungicidal and free radical scavenging agents, we synthesized a focused library of 2-chloroquinoline based monocarbonyl analogs of curcumin (MACs). The synthesized MACs were evaluated for in vitro antifungal and antioxidant activity. The antifungal activity was evaluated against
Santosh Kumar et al.
International journal of biological macromolecules, 49(3), 356-361 (2011-06-07)
This paper describes an elegant cross-linking technique for the preparation of chitosan-chloroquinoline derivative by using a greener technique. Chitosan solution in aqueous acetic acid was treated with 2-chloroquinoline-3-carbaldehyde solution to form hydrogel; the resulting hydrogel was subjected to solvent exchange.
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