CAS 676-10-8
:(T-4)-(N-Butyl-1-butanamine)trifluoroboron
Description:
(T-4)-(N-Butyl-1-butanamine)trifluoroboron, with the CAS number 676-10-8, is a chemical compound that features a trifluoroboron group attached to a butylamine structure. This compound typically exhibits characteristics associated with amines, such as basicity and the ability to form hydrogen bonds, which can influence its solubility in various solvents. The presence of the trifluoroboron moiety imparts unique reactivity, particularly in coordination chemistry, where it can act as a Lewis acid. This compound may also display specific physical properties, including a distinct boiling point and melting point, influenced by its molecular structure. Additionally, due to the trifluoroboron group, it may exhibit enhanced stability and reactivity under certain conditions, making it of interest in various chemical applications, including catalysis and materials science. Safety data should be consulted, as with any chemical, to understand its handling and potential hazards.
Formula:C8H19BF3N
InChI:InChI=1S/C8H19BF3N/c1-3-5-7-13(8-6-4-2)9(10,11)12/h13H,3-8H2,1-2H3
InChI key:InChIKey=WZBJBSCOFNXORT-UHFFFAOYSA-N
SMILES:[NH]([B+3]([F-])([F-])[F-])(CCCC)CCCC
Synonyms:- Borane, trifluoro-, compd. with N-butyl-1-butanamine (1:1)
- Dibutylamine, compd. with BF3 (1:1)
- Dibutylamine, compd. with boron fluoride (BF3) (1:1)
- Boron, (N-butyl-1-butanamine)trifluoro-, (T-4)-
- 1-Butanamine, N-butyl-, compd. with trifluoroborane (1:1)
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