基本情報
- CAS
20440-95-3- 標準SMILES
Cc1ccc(N(c2ccccc2)c2ccc(C)cc2)cc1- InChIKey
YWKKLBATUCJUHI-UHFFFAOYSA-N- 分子式
- C20H19N
- 平均分子量
- 273.4 g/mol
- 単同位体質量
- 273.15174961
名称と識別子
- 優先名称
- 4-Methyl-N-(4-methylphenyl)-N-phenylbenzenamine
- IUPAC
- 4-methyl-N-(4-methylphenyl)-N-phenylaniline
- 現地名
- 4,4'-ジメチルトリフェニルアミン
- 英語名
- 4,4'-Dimethyltriphenylamine
- 分子式
- C20H19N
- 分子量
- 273.37
名称と別名
名称をさらに表示
データベース識別子
- CAS
20440-95-3- PubChem CID
- 88539
- DTXSID
DTXSID5066611- UNII
- J37MWM8NNF
- EC Number
- 243-822-7
- Nikkaji
- J134.870A
物性
構造計算による物性
- XLogP
- 6.5
- 極性表面積
- 3.2 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 1
- 回転可能結合数
- 3
- 重原子数
- 21
- 形式電荷
- 0
- 複雑度
- 269
物理化学的性質
- 融点
- 112 °C · 112°C
- 沸点
- 289.3 °C · 289.3 °C
- 比重(密度)
- 1.079 · 1.079±0.06 g/cm3(Predicted)
- 貯蔵温度
- Sealed in dry,Room Temperature
- 外見
- powder to crystal
- 酸解離定数(Pka)
- -2.19 · -2.19±0.50(Predicted)
- 色
- White to Orange to Green
- InChI
- InChI=1S/C20H19N/c1-16-8-12-19(13-9-16)21(18-6-4-3-5-7-18)20-14-10-17(2)11-15-20/h3-15H,1-2H3
- InChIKey
- YWKKLBATUCJUHI-UHFFFAOYSA-N
- SMILES
- C1(N(C2=CC=C(C)C=C2)C2=CC=CC=C2)=CC=C(C)C=C1
- CAS データベース
- 20440 · 20440-95-3(CAS DataBase Reference)
- EPAの化学物質情報
- 4 · Benzenamine, 4-methyl-N-(4-methylphenyl)-N-phenyl- (20440-95-3)
化学的性質
化学的特性White to yellow solid
安全と法規制
GHS分類
GHS Classification
Warning
H302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P273, P301+P317, P330, P391, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
安全データ
- tsca
- TSCA listed
- hs_code
- 29214990
化学と産業
用途と製造
応用分野
使用4,4'-Dimethyltriphenylamine (DMTPA) can be used as a starting material for the synthesis of 4-[bis(4-methylphenyl)amino]benzaldehyde (BMABA). BMABA is a molecule exhibiting mechanophluorescence, and it has applications in fields such as sensors, data storage and smart switches [5]. The reaction process and mechanism are as follows:This synthesis method is carried out via the Vilsmeier-Haack reaction. DMTPA (1.37 g, 5.01 mmol) was dissolved in DMF (2.3 mL, 29.8 mmol), and trichlorooxaphosphorane (0.46 mL, 5.02 mmol) was slowly added under an ice-water bath. Upon completion of the addition, the reaction temperature was adjusted to 100 °C and the mixture was heated for 3 h. After cooling to room temperature, the product was dissolved in dichloromethane, then neutralised with a sodium bicarbonate solution, extracted, dried over anhydrous Na₂SO₄, and the solid product was collected by vacuum distillation. Chromatographic separation was performed on a silica gel column using a mobile phase of dichloromethane and methanol (Vdichloromethane:Vmethanol = 100:1), yielding pale yellow BMABA (1.14 g, 75.6% yield).
調製方法
純化方法Crystallise the amine once from EtOAc, then twice from EtOH to give pale yellow needles [Marsden J Chem Soc 627 1937, Beilstein 12 III 2033.]
上流・下流製品情報
上流原料
サプライヤー100 社
関連反応
化合物ノート
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