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检测方案
95%
mp
105-112 °C (lit.)
SMILES字符串
COc1c(F)c(F)cc(C(O)=O)c1F
InChI
1S/C8H5F3O3/c1-14-7-5(10)3(8(12)13)2-4(9)6(7)11/h2H,1H3,(H,12,13)
InChI key
YVJHZWWMKFQKDC-UHFFFAOYSA-N
一般描述
2,4,5-Trifluoro-3-methoxybenzoic acid readily forms organotin(IV) complexes.
应用
2,4,5-Trifluoro-3-methoxybenzoic acid may be used as a precursor for the preparation of quinolone derivatives. It may also be used to synthesize 1-(carboxymethyl)-6,7-difluoro-8-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid and triaqua (1,10-phenanthroline-κ2N, N′)(2, 4, 5-trifluoro-3-methoxybenzoato-κO1) cobalt (II) 2, 4, 5-trifluoro-3-methoxybenzoate.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
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
法规信息
新产品
One-pot synthesis and antimicrobial activity of novel quinolone heterocyclic derivatives.
Zheng H, et al.
Journal of Heterocyclic Chemistry, 47(6), 1411-1414 (2010)
Syntheses and crystal structures of di-and triorganotin (IV) derivatives with 2, 4, 5-trifluoro-3-methoxybenzoic acid.
Ma CL, et al.
Polyhedron, 25(17), 3405-3412 (2006)
Crystal structure of triaqua (1, 10-phenanthroline-?2N, N')(2, 4, 5-trifluoro-3-methoxybenzoato-?O1) cobalt (II) 2, 4, 5-trifluoro-3-methoxybenzoate.
Sun J.
Acta Crystallographica Section E, Structure Reports Online, 70(11), m367-m368 (2014)
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