723614

4-(Diphenylamino)phenylboronic acid pinacol ester

95%

• Szinonimák: N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-N-phenylbenzenamine, Diphenyl-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amine
• Tapasztalati képlet (Hill-képlet): C₂₄H₂₆BNO₂
• Molekulatömeg: 371.28
• MDL-szám: MFCD13195770
• UNSPSC kód: 12352103
• PubChem Substance ID: 329764021
• NACRES: NA.23

Tulajdonságok

• Minőségi szint: 100
• Teszt: 95%
• form: powder
• mp: 93-98 °C
• SMILES string: 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
• Nemzetközi kémiai azonosító kulcs: VKSWIFGDKIEVFZ-UHFFFAOYSA-N

Leírás

Általános leírás

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.

Alkalmazás

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).

Biztonsági adatok

• Tárolási osztály kódja: 11 - Combustible Solids
• WGK: WGK 3
• Lobbanási pont (F): Not applicable
• Lobbanási pont (C): Not applicable