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562351

Sigma-Aldrich

4-(N-Boc-amino)phenylboronic acid pinacol ester

97%

Synonym(s):

4-N-Boc-phenylboronic acid pinacol ester, tert-Butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate

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About This Item

Empirical Formula (Hill Notation):
C17H26BNO4
CAS Number:
330793-01-6
Molecular Weight:
319.20
MDL number:
MFCD02179439
UNSPSC Code:
12352103
PubChem Substance ID:
24880027
NACRES:
NA.22

Quality Level

100

assay

97%

form

solid

mp

167-170 °C (lit.)

functional group

amine

SMILES string

CC(C)(C)OC(=O)Nc1ccc(cc1)B2OC(C)(C)C(C)(C)O2

InChI

1S/C17H26BNO4/c1-15(2,3)21-14(20)19-13-10-8-12(9-11-13)18-22-16(4,5)17(6,7)23-18/h8-11H,1-7H3,(H,19,20)

InChI key

HSJNIOYPTSKQBD-UHFFFAOYSA-N

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCP1364
MKCF8294
MKBK1240V
MKBH5264V
MKBF3513

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Articles

Boronic Acid Esters

The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.

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