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| Product | Description | |
|---|---|---|
| 4-(Diphenylamino)phenylboronic acid | 4-(Diphenylamino)phenylboronic acid. Group: Salt other electronic materials. Alternative Names: 4-(N, N-Diphenylamino)-1-phenylboronicacid, 4-(N, N-Diphenylamino)phenylboronicacid, 4-(N-Diphenylamino)phenylboronicacid, 4-(Diphenylamino)benzeneboronicacid, Triphenylamine-4-boronicacid. CAS No. 201802-67-7. Product ID: [4-(N-phenylanilino)phenyl]boronicacid. Molecular formula: 289.1. Mole weight: C18H16BNO2. B (C1=CC=C (C=C1)N (C2=CC=CC=C2)C3=CC=CC=C3) (O)O. InChI=1S/C18H16BNO2/c21-19 (22) 15-11-13-18 (14-12-15) 20 (16-7-3-1-4-8-16) 17-9-5-2-6-10-17/h1-14, 21-22H. TWWQCBRELPOMER-UHFFFAOYSA-N. 95%+. |  |
| 4-(Diphenylamino)phenylboronic acid | ?95%. Group: Organometallic reagents. |  |
| 4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride) | 4-(Diphenylamino)phenylboronic Acid (contains varying amounts of Anhydride). Group: Small molecule semiconductor building blocks. Alternative Names: Triphenylamine-4-boronic Acid (contains varying amounts of Anhydride). CAS No. 201802-67-7. Product ID: [4-(N-phenylanilino)phenyl]boronic acid. Molecular formula: 289.14. Mole weight: C18H16BNO2. B (C1=CC=C (C=C1)N (C2=CC=CC=C2)C3=CC=CC=C3) (O)O. InChI=1S/C18H16BNO2/c21-19 (22) 15-11-13-18 (14-12-15) 20 (16-7-3-1-4-8-16) 17-9-5-2-6-10-17/h1-14, 21-22H. TWWQCBRELPOMER-UHFFFAOYSA-N. | |
| 4-(Diphenylamino)phenylboronic Acid, (contains varying amounts of Anhydride) | 4-(Diphenylamino)phenylboronic Acid, (contains varying amounts of Anhydride). Group: Electroluminescence materials. CAS No. 201802-67-7. Product ID: [4-(N-phenylanilino)phenyl]boronic acid. Molecular formula: 289.1g/mol. Mole weight: C18H16BNO2. B (C1=CC=C (C=C1)N (C2=CC=CC=C2)C3=CC=CC=C3) (O)O. InChI=1S/C18H16BNO2/c21-19 (22) 15-11-13-18 (14-12-15) 20 (16-7-3-1-4-8-16) 17-9-5-2-6-10-17/h1-14, 21-22H. TWWQCBRELPOMER-UHFFFAOYSA-N. | |
| 4-(Diphenylamino)phenylboronic acid pinacol ester | 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. Uses: 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). Group: Synthetic tools and reagents. Alternative Names: 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. Pack Sizes: Packaging 1, 5 g in glass bottle. Product ID: N,N-diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline. Molecular formula: 371.28. Mole weight: C24H26BNO2. CC1 (C)OB (OC1 (C)C)c2ccc (cc2)N (c3ccccc3)c4ccccc4. 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. VKSWIFGDKIEVFZ-UHFFFAOYSA-N. | |
| 4-(Diphenylamino)phenylboronic acid pinacol ester | 95%. Group: Synthetic tools and reagents. | |
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