163244
Butylboronic acid
97%
Synonym(s):
1-Butaneboronic acid
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About This Item
Linear Formula:
CH3(CH2)3B(OH)2
CAS Number:
Molecular Weight:
101.94
Beilstein:
1733489
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
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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Application
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Journal of the American Chemical Society, 116, 3151-3151 (1994)
Tetrahedron Letters, 35, 4419-4419 (1994)
Bioorganic & Medicinal Chemistry Letters, 2, 1391-1391 (1992)
F Ramos et al.
Journal of chromatography. B, Biomedical sciences and applications, 716(1-2), 366-370 (1998-11-21)
A derivatization procedure for confirmatory residue analysis of beta2-agonists is described. Methyl (MBA) and butyl (BBA) boronic acids are simultaneously used for the derivatization of tulobuterol, mabuterol, mapenterol, salbutamol, clenproperol, clenbuterol, clenpenterol and bromobuterol by GC-MS determination. A temperature of
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
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