所有图片(1)
About This Item
经验公式（希尔记法）:
C6H13BF3N
CAS号:
分子量:
166.98
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22
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形狀
solid
mp
134-149 °C
SMILES 字串
F[B-](F)(F)C[NH+]1CCCCC1
InChI
1S/C6H12BF3N/c8-7(9,10)6-11-4-2-1-3-5-11/h1-6H2/q-1/p+1
InChI 密鑰
PFMNVTAJBBIDDU-UHFFFAOYSA-O
應用
(Piperidinium-1-ylmethyl)trifluoroborate can be used as a reagent in the palladium-catalyzed Suzuki-cross coupling reaction with aryl and heteroaryl halides/mesylates to prepare methylpiperidinyl derivatives.
Organotrifluoroborate involved in Suzuki-Miyaura cross-coupling and cross coupling with mesylated phenol derivatives
Organotrifluoroborates as versatile and stable boronic acid surrogates.
Organotrifluoroborates as versatile and stable boronic acid surrogates.
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Reinvestigation of aminomethyltrifluoroborates and their application in Suzuki- Miyaura cross-coupling reactions
Raushel J, et al.
The Journal of Organic Chemistry, 76(8), 2762-2769 (2011)
Cross-coupling of mesylated phenol derivatives with potassium ammonio-and amidomethyltrifluoroborates
Molander GA and Beaumard F
Organic Letters, 13(5), 1242-1245 (2011)
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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