분석
95%
형태
solid
mp
283-290 °C
SMILES string
[K+].F[B-](F)(F)c1cn(c2ccccc12)S(=O)(=O)c3ccccc3
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
InChI key
XLOGEONPZAROPE-UHFFFAOYSA-N
애플리케이션
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.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2, 1-Borazaronaphthalenes
The Journal of Organic Chemistry, 82(1), 549-555 (2017)
Oxyallyl Cation Capture via Electrophilic Deborylation of Organoboronates: Access to α , α `-Substituted Cyclic Ketones
Organic Letters, 21(19), 7837-7840 (2019)
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
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