추천 제품
분석
97%
mp
90-92 °C (lit.)
SMILES string
CCCCB(O)O
InChI
1S/C4H11BO2/c1-2-3-4-5(6)7/h6-7H,2-4H2,1H3
InChI key
QPKFVRWIISEVCW-UHFFFAOYSA-N
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애플리케이션
A precursor to unsymmetric borinic acids, inhibitors of serine proteases. Reagent used to prepare chiral oxazaborolidines.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Journal of the American Chemical Society, 116, 3151-3151 (1994)
Tetrahedron Letters, 35, 4419-4419 (1994)
Bioorganic & Medicinal Chemistry Letters, 2, 1391-1391 (1992)
J O Baker et al.
Biochemical and biophysical research communications, 130(3), 1154-1160 (1985-08-15)
The transition-state-analog inhibitor, 1-butaneboronic acid, markedly enhances the uptake of one g-atom of Zn2+ ions from a metal ion buffer system by Zn-depleted Aeromonas aminopeptidase. In contrast, a substrate-analog inhibitor, n-valeramide, does not perturb the equilibrium between Zn2+ ions and
M Inouye et al.
Japanese journal of medicine, 27(1), 29-33 (1988-02-01)
A highly sensitive and specific quantitative assay for inositol in serum has been developed. Uremic serum, to which hexahydroxybenzene as an internal standard was added, was deproteined with trichloroacetate. The supernatant aqueous phase was taken after lipids in serum were
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