4-(Diphenylamino)phenylboronic acid pinacol ester

Cat.No ACMA00016287

Basic Information Description Application Features And Benefits

Catalog Number	ACMA00016287
Synonyms	Diphenyl-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amine, N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-N-phenylbenzenamine
IUPAC Name	N,N-diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Molecular Weight	371.28
Molecular Formula	C24H26BNO2
Canonical SMILES	CC1(C)OB(OC1(C)C)c2ccc(cc2)N(c3ccccc3)c4ccccc4
InChI	1S/C24H26BNO2/c1-23(2)24(3,4)28-25(27-23)19-15-17-22(18-16-19)26(20-11-7-5-8-12-20)21-13-9-6-10-14-21/h5-18H,1-4H3
InChI Key	VKSWIFGDKIEVFZ-UHFFFAOYSA-N
Melting Point	93-98 °C
Storage	room temp
Assay	95%
MDL Number	MFCD13195770
NACRES	NA.23
Packaging	Packaging 1, 5 g in glass bottle
PubChem ID	329764021
Quality Level	100

Description 4-(Diphenylamino)phenylboronic acid pinacol ester is an aryl boronic acid ester that is majorly used in organic synthesis. It can be used in the transition metal-catalyzed Suzuki-Miyaura cross-coupling reaction due to its low toxicity and unique reactivity. It is an electron rich boronic acid ester that can also be used in protodeboronation.

Application 4-(Diphenylamino)phenylboronic acid pinacol ester may be used to synthesize 4-(2,2' -bithiophen-5-yl)- 5-phenylpyrimidine for potential usage in the development of sensing devices for the detection of nitroaromatic explosives. It can also be used in the synthesis of oligothiophene (electron donating group) for the fabrication of dye sensitized solar cells (DSSCs).

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