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| Product Name: | 2,6-Diisopropylaniline | | Synonyms: | Amitraz E.C.;2,6-Diisopropylaniline, 90+%;Boc-D-Ala(beta-cyclobutyl)-OH·Diisopropylaniline,90%;2,6-diisopropyl-anilin;2,6-diisopropylphenylamine;Aniline, 2,6-diisopropyl-;2,6-DIISOPROPYLANILINE, TECH., 90% | | CAS: | 24544-04-5 | | MF: | C12H19N | | MW: | 177.29 | | EINECS: | 246-305-4 | | Product Categories: | Amines;Aniline Derivatives;C11 to C38;Nitrogen Compounds;o-alkylated Anilines;Building Blocks;C12;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Piperidines ,Homopiperidines;bc0001 | | Mol File: | 24544-04-5.mol |
| 2,6-Diisopropylaniline Chemical Properties |
| 2,6-Diisopropylaniline Usage And Synthesis |
| Description | 2,6-Diisopropylaniline is an organic compound with the formula H2NC6H3(CHMe2)2 (Me = CH3). It is a colorless liquid although, like many anilines, samples can appear yellow or brown.
| | Chemical Properties | Clear liquid | | Uses | 2,6-Diisopropylaniline is used as intermediate for the manufacture of carbodiimides stabilizers, RIM-PUR, synthetic resins, pesticides, antioxidants, pharmaceuticals and other products.
2,6-Diisopropylaniline may be used in the preparation of multitopic Schiff-base ligand precursors.It may be used in the preparation of NSN-donor proligand, 4,5-bis(2,6-diisopropylanilino)-2,7-di-tert-butyl-9,9-dimethylthioxanthene. It may be used to prepare N-heterocyclic carbene complexes for α-arylation of acyclic ketones, amination of haloarenes, and aqueous Suzuki coupling.
2,6-Diisopropylaniline may be used in the preparation of organocatalyst based on naphthalene diimides (NDIs).
| | Uses | 2,6-Diisopropylaniline acts as an intermediate used in the production of carbodiimides stabilizers, synthetic resins, antioxidants and active pharmaceutical ingredients. It is also used in the preparation of multitopic Schiff-base ligand precursors and 4,5-bis(2,6-diisopropylanilino)-2,7-di-tert-butyl-9,9-dimethylthioxanthene. It also undergoes condensation reaction with triacetylmethane to get -[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione. Further, it is used to prepare N-heterocyclic carbene complexes for alfa-arylation of acyclic ketones, amination of haloarenes and aqueous Suzuki coupling. In addition to this, it is used in the prepartion of organocatalyst based on naphthalene diimides. | | Uses | 2,6-Diisopropylaniline was used in the preparation of multitopic Schiff-base ligand precursors. It was also used in the preparation of NSN-donor proligand, 4,5-bis(2,6-diisopropylanilino)-2,7-di-tert-butyl-9,9-dimethylthioxanthene. | | Reactions | 2,6-Diisopropylaniline is an amine. It undergoes condensation with triacetylmethane in toluene in the presence of p-toluenesulfonic acid provides 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione.
2,6-Diisopropylaniline is an aromatic amine. It reacts with bis(trimethylsilylmethyl)yttrium complexes supported by bulky amidopyridinate (Ap) and amidinate (Amd) ligands to afford yttrium alkyl anilido species. This reaction involves the elimination of TMS (Trimethylsilane). | | General Description | 2,6-Diisopropylaniline is an aromatic amine. It reacts with bis(trimethylsilylmethyl)yttrium complexes supported by bulky amidopyridinate (Ap) and amidinate (Amd) ligands to afford yttrium alkyl anilido species. This reaction involves the elimination of TMS (Trimethylsilane). |
| 2,6-Diisopropylaniline Preparation Products And Raw materials |
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