163244
Butylboronic acid
97%
Synonym(s):
1-Butaneboronic acid
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All Photos(3)
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
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Bioorganic & Medicinal Chemistry Letters, 2, 1391-1391 (1992)
B Bennett et al.
Biochemistry, 36(32), 9837-9846 (1997-08-12)
The Co(II)Zn(II)- and Zn(II)Co(II)-substituted derivatives of the aminopeptidase from Aeromonas proteolytica (AAP) were probed by EPR spectroscopy. EPR spectra of the high-spin S = 3/2 Co(II) ions in [CoZn(AAP)] and [ZnCo(AAP)] indicated that each metal binding site provides a spectroscopically
Determination of meprobamate as an n-butylboronate ester derivative in serum by gas-liquid chromatography.
B Johansson et al.
Journal of chromatography, 341(2), 462-464 (1985-06-14)
Measurement of myo-inositol in diabetic sera by GC/MS/SIM using n-butylboronate derivatives.
M Hasegawa et al.
Clinica chimica acta; international journal of clinical chemistry, 176(2), 207-212 (1988-08-31)
G E Joannou et al.
Steroids, 61(1), 11-17 (1996-01-01)
We report the synthesis of 3 beta,15 beta,17 alpha-trihydroxy-5-pregnen-20- one (1) from 3 beta,15 beta-dihydroxy-5,16-pregnadien-20-one (11) in 7 steps using boronate derivatives as a means of protecting the 17,20-glycol side-chain of steroid intermediates. 16 alpha,17 alpha-Epoxy-3 beta,15 beta-dihydroxy-5- pregnen-20-one (12)
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