추천 제품
Quality Level
분석
≥97.0% (T)
형태
crystals
포함
1-3% ether as stabilizer
solubility
methylene chloride: 20 mg/mL, clear, colorless
저장 온도
2-8°C
SMILES string
F[B-](F)(F)F.CC[O+](CC)CC
InChI
1S/C6H15O.BF4/c1-4-7(5-2)6-3;2-1(3,4)5/h4-6H2,1-3H3;/q+1;-1
InChI key
IYDQMLLDOVRSJJ-UHFFFAOYSA-N
애플리케이션
Triethyloxonium tetrafluoroborate can be used:
- To prepare amino esters by reacting with lactams followed by hydrolysis.
- In the preparation of substituted imidazolines from aziridines and nitriles via [3+2]-cycloaddition reaction.
- For the N-alkylation of a series of N-arylsulfonyl-α-amino acid methyl esters having variable substituents at 4th position of the sulfonamide aromatic ring.
기타 정보
Powerful ethylating agent; Esterification of acids; Modifies carboxyl residues in proteins
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
보충제 위험성
Storage Class Code
8A - Combustible, corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Choose from one of the most recent versions:
이미 열람한 고객
Synthesis of substituted imidazolines via [3+ 2]-cycloaddition of aziridines with nitriles
Tetrahedron Letters, 45(6), 1137-1141 (2004)
The Journal of Organic Chemistry, 42, 1801-1801 (1977)
The identification of aspartic acid residue 52 as being critical to lysozyme activity.
Biochemistry, 8(10), 4199-4205 (1969-10-01)
The Journal of Organic Chemistry, 44, 1149-1149 (1979)
Angewandte Chemie (International Edition in English), 72, 927-927 (1960)
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