すべての製品
CAS: 24544-04-5 2,6-Diisopropylaniline for Herbicide, acaricide, fungicide intermediate
| 起源の場所 | 中国 |
|---|---|
| ブランド名 | HOYOSHEE |
| 証明 | ISO9001 |
| モデル番号 | HYX-18-7 |
| 最小注文数量 | 交渉 |
| 価格 | 交渉可能 |
| パッケージの詳細 | 25KGドラム |
| 受渡し時間 | 5～8日 |
| 支払条件 | L/C、D/A、D/P、T/T、ウェスタンユニオン |
| 供給の能力 | 500トン/月 |
商品の詳細
| CAS | 24544-04-5 | MF | C12H19N |
|---|---|---|---|
| 融点 | -45 °C (点灯) | 沸点 | 257 °C (点灯) |
| 密度 | 25 °C で 0.94 g/mL (点灯) | 蒸気圧 | <0> |
| 形状 | 液体 | ||
| ハイライト | 2,6-Diisopropylaniline herbicide intermediate,2 |
||
製品の説明
CAS: 24544-04-5
Product: 2,6-Diisopropylaniline for Herbicide, Acaricide, Fungicide Intermediate
Product: 2,6-Diisopropylaniline for Herbicide, Acaricide, Fungicide Intermediate
Product Overview
2,6-Diisopropylaniline is an organic compound with the formula H₂NC₆H₃(CHMe₂)₂ (Me = CH₃). It typically appears as a colorless liquid, though samples may exhibit yellow or brown coloration due to oxidation, which is common among aniline compounds.
Chemical Properties
Clear liquid formulation suitable for industrial applications.
Industrial Applications
2,6-Diisopropylaniline serves as a versatile intermediate in the manufacturing of:
- Carbodiimides stabilizers
- RIM-PUR systems
- Synthetic resins
- Pesticides, herbicides, acaricides, and fungicides
- Antioxidants
- Pharmaceutical compounds
- Various specialty chemical products
Specific Chemical Uses
This compound finds application in the preparation of:
- Multitopic Schiff-base ligand precursors
- NSN-donor proligand, 4,5-bis(2,6-diisopropylanilino)-2,7-di-tert-butyl-9,9-dimethylthioxanthene
- N-heterocyclic carbene complexes for α-arylation of acyclic ketones
- Amination of haloarenes and aqueous Suzuki coupling reactions
- Organocatalysts based on naphthalene diimides (NDIs)
Chemical Reactions
As an aromatic amine, 2,6-Diisopropylaniline undergoes condensation with triacetylmethane in toluene in the presence of p-toluenesulfonic acid to yield 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione. It also reacts with bis(trimethylsilylmethyl)yttrium complexes supported by bulky amidopyridinate (Ap) and amidinate (Amd) ligands to form yttrium alkyl anilido species, with elimination of trimethylsilane (TMS).
Purification Methods
The purification process involves contacting 2,6-diisopropylaniline with an alkyl- or arylsulfonic acid to produce the corresponding sulfonic acid salt, recrystallizing the salt in an organic solvent, and subsequently treating the obtained crystals with an alkali to regenerate the purified compound.
Raw Materials & Preparation Products
| Raw Materials | Preparation Products |
|---|---|
| Isoproturon → 2-Isopropylaniline | 3,5-diisopropylphenol 4,4'-Methylenebis(2,6-diisopropylaniline) 1,3-diisopropyl-2-isothiocyanato-5-phenoxybenzene (2,6-Diisopropyl-4-Phenoxy)Phenylthiourea Diafenthiuron 4-Phenoxy-2,6-Diisopropyl Aniline 2,6-Diisopropylphenyl isocyanate N-Cyclohexyl-2,6-bis(1-methylethyl)-Benzenamine 2,4-Diisopropylbenzene-1,3-diamine 2-(2,6-diisopropylphenyl)-1H-benzo[5,10]anthra[2,1,9-def]isoquinoline-1,3(2H)-dione |
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