所有图片(1)
About This Item
经验公式(希尔记法):
C7H4BF4KO
CAS号:
分子量:
230.01
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
表单
solid
mp
230-235 °C
官能团
aldehyde
fluoro
SMILES字符串
[K+].Fc1ccc(C=O)cc1[B-](F)(F)F
InChI
1S/C7H4BF4O.K/c9-7-2-1-5(4-13)3-6(7)8(10,11)12;/h1-4H;/q-1;+1
InChI key
HCTPXGYDPRWOOU-UHFFFAOYSA-N
应用
Organotrifluoroborate involved in:
Organotrifluoroborates as versatile and stable boronic acid surrogates.
- Metal-free chlorodeboronation
- Hydrolysis via silica gel and water
- Suzuki-Miyaura reactions
- Reductive amination
- Wittig reactions
Organotrifluoroborates as versatile and stable boronic acid surrogates.
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
商品
Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.
相关内容
These bench stable Potassium Organotrifluoroborates are useful for Suzuki-Miyaura cross-coupling reactions and have also been used for a variety of other C-C bond forming reactions. Importantly, these reagents are compatible with a wide range of functional groups and are stable to many commonly used and harsh reaction conditions.
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