2,4-二氯苯甲酰氯
一般危化品
2,4-二氯苯甲酰氯结构式
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常用名 | 2,4-二氯苯甲酰氯 | 英文名 | 2,4-Dichlorobenzoyl chloride |
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| CAS号 | 89-75-8 | 分子量 | 209.457 | |
| 密度 | 1.5±0.1 g/cm3 | 沸点 | 251.8±20.0 °C at 760 mmHg | |
| 分子式 | C7H3Cl3O | 熔点 | 28 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 103.4±22.3 °C | |
| 符号 |
GHS05, GHS07 |
信号词 | Danger |
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Synthesis and pharmacological evaluation of a new class of peroxisome proliferator-activated receptor modulators.
Bioorg. Med. Chem. Lett. 12(24) , 3565-7, (2002) A series of 5-substituted 2-benzoylaminobenzoic acids has been synthesized and assayed for PPARalpha/gamma activity. Both dual activators and selective PPARgamma agonists have been identified. This class of compounds was shown to activate the PPARgamma recept... |
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NADPH-dependent reductive ortho dehalogenation of 2,4-dichlorobenzoic acid in Corynebacterium sepedonicum KZ-4 and Coryneform bacterium strainNTB-1 via 2,4-dichlorobenzoyl coenzyme A.
J. Bacteriol. 178(9) , 2656-61, (1996) Corynebacterium sepedonicum KZ-4, described earlier as a strain capable of growth on 2,4-dichlorobenzoate (G.M. Zaitsev and Y.N. Karasevich, Mikrobiologiya 54:356-369, 1985), is known to metabolize this substrate via 4-hydroxybenzoate and protocatechuate, and... |
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Synthesis and SAR of GlyT1 inhibitors derived from a series of N-((4-(morpholine-4-carbonyl)-1-(propylsulfonyl)piperidin-4-yl)methyl)benzamides.
Bioorg. Med. Chem. Lett. 16(23) , 5968-72, (2006) This Letter describes the synthesis and SAR, developed through an iterative analog library approach, of potent and selective non-sarcosine-derived GlyT1 inhibitors. |