C70401
2-氯喹啉
99%
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C9H6ClN
化学文摘社编号:
分子量:
163.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-317-8
Beilstein/REAXYS Number:
112561
MDL number:
产品名称
2-氯喹啉, 99%
InChI key
OFUFXTHGZWIDDB-UHFFFAOYSA-N
InChI
1S/C9H6ClN/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H
SMILES string
Clc1ccc2ccccc2n1
assay
99%
form
crystals
bp
266-267 °C (lit.)
mp
34-37 °C (lit.)
density
1.23 g/mL at 25 °C (lit.)
Quality Level
正在寻找类似产品? 访问 产品对比指南
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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
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
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.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持