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CAS 330793-01-6

N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline TCI B5588

N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline TCI B5588

Chemical Identity

Other names
N-Boc-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline · 4-[(tert-Butoxycarbonyl)amino]phenylboronic Acid Pinacol Ester · 4-(Boc-amino)phenylboronic Acid Pinacol Ester · tert-Butyl [4-(4,4,5,5-Tetr
CAS No.
330793-01-6
PubChem
CID 2734617·SID 354335159
Formula
C17H26BNO4
Molecular weight
319.21 g/mol
Purity
>99.0%(HPLC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)NC(=O)OC(C)(C)C
InChIKey
HSJNIOYPTSKQBD-UHFFFAOYSA-N
MDL
MDL02179439
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N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile organoboron reagent featuring a Boc-protected aniline coupled with a pinacol boronate ester, primarily utilized as a key building block in Suzuki-Miyaura cross-coupling reactions. This compound enables the efficient synthesis of biaryl amine derivatives, which are essential structural motifs in medicinal chemistry and drug discovery programs. Its dual functionality — a protected amine and a reactive boronate — makes it an ideal intermediate for multi-step organic syntheses requiring orthogonal reactivity.

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