480053
4-tert-Butylphenylboronic acid
≥95.0%
Synonym(s):
(p-tert-Butylphenyl)boronic acid, 4-t-Butylbenzeneboronic acid, 4-t-Butylphenylboronic acid, 4-tert-Butylbenzeneboronic acid, p-tert-Butylbenzeneboronic acid, [4-(1,1-Dimethylethyl)phenyl]boronic acid
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About This Item
Linear Formula:
(CH3)3CC6H4B(OH)2
CAS Number:
Molecular Weight:
178.04
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥95.0%
mp
191-196 °C (lit.)
SMILES string
CC(C)(C)c1ccc(cc1)B(O)O
InChI
1S/C10H15BO2/c1-10(2,3)8-4-6-9(7-5-8)11(12)13/h4-7,12-13H,1-3H3
InChI key
MNJYZNVROSZZQC-UHFFFAOYSA-N
Related Categories
Application
Cross-coupling building block used in synthesis of tetracycline derivatives.
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
Regulatory Information
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The Journal of Organic Chemistry, 68, 10199-10199 (2003)
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The design and synthesis of two families of molecular-gear prototypes is reported, with the aim of assembling them into trains of gears on a surface and ultimately achieving controlled intermolecular gearing motion. These piano-stool ruthenium complexes incorporate a hydrotris(indazolyl)borate moiety
Xiao Yan et al.
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Unveiling the reaction mechanism is significant for developing high-performance catalysts. In this paper, a series of precisely controlled PdxM147-x (M = Cu, Pt, Au, Rh, Ru) dendrimer encapsulated nanoparticles (DENs) has been successfully synthesized. The mechanisms of PdxM147-x as catalysts
Heng Wang et al.
Chirality, 27(8), 523-531 (2015-04-25)
A novel pyridineoxazoline (PyOx) containing helical polymer, poly{(-)-(S)-4-tert-butyl-2-[5-(4-tert-butylphenyl)-3-vinylpyridin-2-yl]-oxazoline} (PA), was designed and synthesized to approach the effect of chain conformation on the catalytic property. Its complex with Cu(OTf)(2) , i.e., Cu(II)-PA, was employed to catalyze the homogeneous Diels-Alder (D-A) reaction
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