质量水平
检测方案
≥95%
形式
powder
mp
217-220 °C (lit.)
SMILES字符串
OB(O)c1cc(cc(c1)C(F)(F)F)C(F)(F)F
InChI
1S/C8H5BF6O2/c10-7(11,12)4-1-5(8(13,14)15)3-6(2-4)9(16)17/h1-3,16-17H
InChI key
BPTABBGLHGBJQR-UHFFFAOYSA-N
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应用
Reactant involved in the synthesis of:
- Methylene-arylbutenones via carbonylative arylation of allenols
- 4-aminoquinoline analogs via Ullman / Suzuki / Negishi coupling
- Primary amino acid derivatives with anticonvulsant activity
- Alkyl arylcarbamates via Cu-catalyzed coupling with potassium cyanate
- Aryl-substituted succinimides and cyclic ketones by asymmetric conjugate addition
- Axially chiral dicarboxylic acids for asymmetric Mannich-type reactions
其他说明
含不定量的酸酐
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Journal of cellular biochemistry, 40(2), 249-260 (1989-06-01)
31P Nuclear Magnetic Resonance (NMR) studies were performed on mono- and diisopropylphosphoryl derivatives of alpha-chymotrypsin, trypsin, and subtilisin. Questions addressed included the pKa of the active center Asp...His...Ser triad in both species. While the pKa in the diisopropylphosphoryl derivatives is
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