(4-Boc-aminophenyl)boronic acid

Names

[ Name ]:
(4-Boc-aminophenyl)boronic acid

[Synonym ]:
MFCD02093054
4-(Boc-amino)phenylboronic Acid
[4-[(2-methylpropan-2-yl)oxycarbonylamino]phenyl]boronic acid
4-(N-Boc-amino)phenylboronic acid
(4-((tert-Butoxycarbonyl)amino)phenyl)boronic acid
Carbamic acid, N-(4-boronophenyl)-, 1,1-dimethylethyl ester
4-(Boc-amino)benzeneboronic Acid
4-[(tert-Butoxycarbonyl)amino]phenylboronic Acid
{4-[(tert-Butoxycarbonyl)amino]phenyl}boronic acid
4-[(tert-Butoxycarbonyl)amino]benzeneboronic Acid
(4-Boc-Aminophenyl)boronic acid
[4-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)phenyl]boronic acid

Biological Activity

[Description]:

(4-Boc-Aminophenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Melting Point ]:
199-204 °C (dec.)(lit.)

[ Molecular Formula ]:
C₁₁H₁₆BNO₄

[ Molecular Weight ]:
237.06

[ Exact Mass ]:
237.117233

[ PSA ]:
78.79000

[ LogP ]:
2.37

[ Index of Refraction ]:
1.531

[ Storage condition ]:
Keep Cold

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
S26-S36/37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2931900090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2931900090

[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Articles

Rhodium-catalyzed asymmetric allylic substitution with boronic acid nucleophiles.

Org. Lett. 8 , 4569, (2006)

An enantio-, regio-, and diastereoselective rhodium(I)-catalyzed desymmetrization of a meso-cyclic allylic dicarbonate with organoboronic acid nucleophiles is described. The rhodium(I) catalyst formed...