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质量水平
方案
97%
表单
solid
mp
82-86 °C (lit.)
储存温度
2-8°C
SMILES字符串
CC(C)(C)OC(=O)n1cc(cn1)B2OC(C)(C)C(C)(C)O2
InChI
1S/C14H23BN2O4/c1-12(2,3)19-11(18)17-9-10(8-16-17)15-20-13(4,5)14(6,7)21-15/h8-9H,1-7H3
InChI key
IPISOFJLWYBCAV-UHFFFAOYSA-N
应用
Reagent used for
Reagent used in Preparation of
- Suzuki Coupling
- Copper-catalyzed azidation
Reagent used in Preparation of
- Selective quinazolinyl-phenol inhibitors of CHK1 as potential antitumors and radioprotectants
- Stereoselective synthesis of selective Cathepsin inhibitors
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
Eyeshields, Gloves, type N95 (US)
Copper(II)-catalyzed conversion of aryl/heteroaryl boronic acids, boronates, and trifluoroborates into the corresponding azides: substrate scope and limitations
K. D. Grimes, et al.,
Synthesis, 9, 1441-1448 (2010)
John J Caldwell et al.
Journal of medicinal chemistry, 54(2), 580-590 (2010-12-29)
Structure-based design was applied to the optimization of a series of 2-(quinazolin-2-yl)phenols to generate potent and selective ATP-competitive inhibitors of the DNA damage response signaling enzyme checkpoint kinase 2 (CHK2). Structure-activity relationships for multiple substituent positions were optimized separately and
Paul A Bethel et al.
Bioorganic & medicinal chemistry letters, 19(16), 4622-4625 (2009-07-21)
A number of molecular recognition features have been exploited in structure-based design of selective Cathepsin inhibitors.
商品
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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