750263
Potassium 1-(phenylsulfonyl)-1H-indole-3-trifluoroborate
95%
别名:
Potassium 1-(phenylsulfonyl)-3-indoletrifluoroborate, Potassium 1-(phenylsulfonyl)-3-indolyltrifluoroborate
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C14H10BF3KNO2S
分子量:
363.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Assay:
95%
Form:
solid
InChI
1S/C14H10BF3NO2S.K/c16-15(17,18)13-10-19(14-9-5-4-8-12(13)14)22(20,21)11-6-2-1-3-7-11;/h1-10H;/q-1;+1
SMILES string
[K+].F[B-](F)(F)c1cn(c2ccccc12)S(=O)(=O)c3ccccc3
InChI key
XLOGEONPZAROPE-UHFFFAOYSA-N
assay
95%
form
solid
mp
283-290 °C
Application
Potassium 1-(phenylsulfonyl)-1H-indole-3-trifluoroborate can be used as a reactant in:
- The palladium-catalyzed Suzuki-Miyaura α-arylation reaction.
- The nucleophilic addition reactions.
- The preparation of indole substituted borazaronaphthalene.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Oxyallyl Cation Capture via Electrophilic Deborylation of Organoboronates: Access to α , α `-Substituted Cyclic Ketones
Nguyen TN, et al.
Organic Letters, 21(19), 7837-7840 (2019)
Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2, 1-Borazaronaphthalenes
Davies GHM, et al.
The Journal of Organic Chemistry, 82(1), 549-555 (2017)
Gary A Molander et al.
The Journal of organic chemistry, 78(8), 4123-4131 (2013-04-11)
A method has been developed for the Pd-catalyzed synthesis of α-(hetero)aryl esters and amides through a Suzuki-Miyaura cross-coupling reaction. This method avoids the use of strong base, does not necessitate inert or low temperature formation of reagents, and does not
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持