4-(Diphenylamino)phenylboronic acid pinacol ester

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.
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
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).
Storage	room temp
Assay	95%
MDL Number	MFCD13195770
NACRES	NA.23
Packaging	Packaging 1, 5 g in glass bottle
Quality Level	100