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- 英文名：
6-Chloro-4-ethynyl-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
168834-32-0
6-Chloro-4-ethynyl-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one
168834-32-0
C₁₁H₅ClF₃NO₂
275.61
No Data Available
No Data Available
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文献和实验6-Chloro-4-ethynyl-1,4-dihydro-4-(trifluoromethyl)-2H-3,1-benzoxazin-2-one
168834-32-0
C₁₁H₅ClF₃NO₂
275.61
No Data Available
No Data Available
Immunochemical Method for Ochratoxin A
Ochratoxin A (7-L-β-phenylalanylcarbonyl-5-chloro-8-hydroxy-3,4-dihydro-3-R-methylisocoumarin, Fig. 1 ) was first isolated in 1965 from A. ochraceus (1 ). Meanwhile several Aspergillus and Penicillium species are known to produce
Molecular Assembly-Assisted Biocatalytic Reactions in Ionic Liquids
. For this approach, we have synthesized a hydrophobic IL [C8 mim][Tf2 N] (1-octyl-3-methyl imidazolium bis(trifluoromethyl sulfonyl) amide) containing a long pendant hydrocarbon chain to facilitate the dissolution of AOT molecules. A detailed description
Overview of Formation of G‐Quadruplex Structures
studied in on quadruplex formation. Chemical formulas of (A ) 6‐Methylguanine, (B ) Inosine, (C ) 6‐Thioguanine, (D ) 8‐Aminoguanine, (E ) 8‐Methylguanine, (F ) 8‐Bromoguanine, and (G ) 7,8‐dihydro‐8‐oxoguanine. Schematic representations of the G
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