推荐产品
质量水平
方案
98%
mp
157-160 °C (lit.)
溶解性
ethanol: soluble 1 g/10 mL, clear, colorless
官能团
carboxylic acid
chloro
SMILES字符串
OC(=O)c1ccc(Cl)cc1Cl
InChI
1S/C7H4Cl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,(H,10,11)
InChI key
ATCRIUVQKHMXSH-UHFFFAOYSA-N
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一般描述
2,4-二氯苯甲酸是太阳辐射驱动光-fenton 降解水中氯苯磷的产物。
应用
采用 2，4-二氯苯甲酸固相萃取，气相色谱法测定地表水中的极性酸性除草剂。在嘧啶并 [2′，1′：2，3] 噻唑并 [4，5-b] 喹喔啉衍生物 的合成中用作试剂。在 1-（取代）-1,4-二氢-6-硝基-4-氧代-7-（次级氨基）-喹啉-3-羧酸的合成过程中，将其用作起始试剂。
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - 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)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Gas chromatographic determination of acid herbicides in surface water samples with electron-capture detection and mass spectrometric confirmation.
Vink M and Van der Poll JM.
Journal of Chromatography A, 733(1), 361-366 (1996)
Sunday A Adebusoye et al.
Bioresource technology, 102(3), 3041-3048 (2010-11-16)
Multiple bacterial strains with CBA metabolic properties were isolated using a simple selective strategy. Phylogenetic analysis of the 16S rRNA gene sequences grouped them into two main clusters consisting of four bacterial phyla and belonging to 17 genera. Whereas growth
G M Zaitsev et al.
FEMS microbiology letters, 65(2), 171-176 (1991-06-15)
The strains of Arthrobacter globiformis KZT1, Corynebacterium sepedonicum KZ4 and Pseudomonas cepacia KZ2 capable of early dehalogenation and complete oxidation of 4-chloro-, 2,4-dichloro-and 2-chlorobenzoic acids, respectively, have been analyzed for the origin of the genetic control of degradation. The occurrence
A Iu Sokolov et al.
Eksperimental'naia i klinicheskaia farmakologiia, 74(5), 13-16 (2011-08-04)
Neurophysiological experiments on anesthetized rats were used to study the effects of various doses (12.5, 25, 37.5 mg/kg, i.v.) of drug composition migrepin (representing a combination of potassium-2,4-dichlorobenzoate, carbamazepine, and caffeine) on background firing of the trigeminal nucleus caudalis neurons
Palaniappan Senthilkumar et al.
European journal of medicinal chemistry, 44(1), 345-358 (2008-05-27)
Various 1-(substituted)-1,4-dihydro-6-nitro-4-oxo-7-(sub-secondary amino)-quinoline-3-carboxylic acids were synthesized from 2,4-dichlorobenzoic acid by six step synthesis. The compounds were evaluated for antimycobacterial in vitro and in vivo against Mycobacterium tuberculosis H37Rv (MTB), multi-drug resistant Mycobacterium tuberculosis (MDR-TB) and Mycobacterium smegmatis (MC(2)) and also
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