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化驗
97%
mp
90-92 °C (lit.)
SMILES 字串
CCCCB(O)O
InChI
1S/C4H11BO2/c1-2-3-4-5(6)7/h6-7H,2-4H2,1H3
InChI 密鑰
QPKFVRWIISEVCW-UHFFFAOYSA-N
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應用
不对称硼酸的前体、丝氨酸蛋白酶抑制剂。用于制备手性噁唑硼烷的试剂。
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
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Bioorganic & Medicinal Chemistry Letters, 2, 1391-1391 (1992)
Journal of the American Chemical Society, 116, 3151-3151 (1994)
Tetrahedron Letters, 35, 4419-4419 (1994)
Michał K Cyrański et al.
The Journal of chemical physics, 128(12), 124512-124512 (2008-04-02)
Boronic acids have emerged as one of the most useful class of organoboron molecules, with application in synthesis, catalysis, analytical chemistry, supramolecular chemistry, biology, and medicine. In this study, the structural and spectroscopic properties of n-butylboronic acid were investigated using
C C De Paola et al.
Biochemistry, 38(28), 9048-9053 (1999-07-22)
Hydrolases containing two metal ions connected by a bridging ligand catalyze reactions important in carcinogensis, tissue repair, post-translational modification, control and regulation of biochemical pathways, and protein degradation. The aminopeptidase from Aeromonas proteolytica serves as a paradigm for the study
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