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565814

Sigma-Aldrich

4-(N-Boc-amino)phenylboronic acid

≥95.0%

Synonym(s):

4-(Boc-amino)phenylboronic acid, 4-[(tert-Butoxycarbonyl)amino]benzeneboronic acid, C-(1,1-Dimethylethyl) N-(4-boronophenyl)carbamate, [4-(N-Bocamino)phenyl]boronic acid, [4-(tert-Butoxycarbonylamino)phenyl]boronic acid, [4-[[[(1,1-Dimethylethyl)oxy]carbonyl]amino]phenyl]boronic acid

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About This Item

Linear Formula:
(CH3)3CO2CNHC6H4B(OH)2
CAS Number:
Molecular Weight:
237.06
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

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List Price$110.00Save 20%
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In StockDetails


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Quality Level

assay

≥95.0%

form

solid

mp

199-204 °C (dec.) (lit.)

functional group

amine

SMILES string

CC(C)(C)OC(=O)Nc1ccc(cc1)B(O)O

InChI

1S/C11H16BNO4/c1-11(2,3)17-10(14)13-9-6-4-8(5-7-9)12(15)16/h4-7,15-16H,1-3H3,(H,13,14)

InChI key

UBVOLHQIEQVXGM-UHFFFAOYSA-N

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This Item
706140417599480053
assay

≥95.0%

assay

97%

assay

≥95.0%

assay

≥95.0%

mp

199-204 °C (dec.) (lit.)

mp

209-214 °C

mp

204-206 °C (lit.)

mp

191-196 °C (lit.)

form

solid

form

powder

form

powder

form

-

functional group

amine

functional group

amide

functional group

-

functional group

-

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

Application

Boronic acid used in a study of the rhodium-catalyzed desymmetrization of a meso-cyclic allylic dicarbonate via SN2′ substitution.[1]

Other Notes

Contains varying amounts of anhydride

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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