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Merck
CN

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
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-607-7
Beilstein/REAXYS Number:
1733489
MDL number:
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InChI key

QPKFVRWIISEVCW-UHFFFAOYSA-N

InChI

1S/C4H11BO2/c1-2-3-4-5(6)7/h6-7H,2-4H2,1H3

SMILES string

CCCCB(O)O

assay

97%

Quality Level

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Application

A precursor to unsymmetric borinic acids, inhibitors of serine proteases. Reagent used to prepare chiral oxazaborolidines.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Bioorganic & Medicinal Chemistry Letters, 2, 1391-1391 (1992)
Journal of the American Chemical Society, 116, 3151-3151 (1994)
Tetrahedron Letters, 35, 4419-4419 (1994)
Alicja J Copik et al.
Inorganic chemistry, 44(5), 1160-1162 (2005-03-01)
Metalloproteases utilize their active site divalent metal ions to generate a nucleophilic water/hydroxide. For methionine aminopeptidases (MetAPs), the exact location of this nucleophile, as well as of the substrate, with respect to the active site metal ion is unknown. In
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

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