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线性分子式:
(CH3)3CC6H4NH2
化学文摘社编号:
分子量:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-215-9
Beilstein/REAXYS Number:
2205786
MDL number:
产品名称
4-叔丁基苯胺, 99%
InChI key
WRDWWAVNELMWAM-UHFFFAOYSA-N
InChI
1S/C10H15N/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7H,11H2,1-3H3
SMILES string
CC(C)(C)c1ccc(N)cc1
assay
99%
form
liquid
refractive index
n20/D 1.538 (lit.)
bp
90-93 °C/3 mmHg (lit.)
mp
15-16 °C (lit.)
density
0.937 g/mL at 25 °C (lit.)
Quality Level
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Application
4-叔丁基苯胺用于合成:
- 4-叔丁基-4′,4″-二硝基三苯胺,含二胺单体的新三苯胺
- 2-氧嘧啶[4,5-d]嘧啶-5(6H)-酮
General description
4-叔丁基苯胺和 4-叔丁基苯甲醛可以通过基质辅助激光解吸电离芯片系统在乙醇中发生席夫碱形成反应。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Self-complementary hydrogen bonding heterocycles designed for the enforced self-assembly into supramolecular macrocycles.
Marsh A, et al.
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Bioorganic & medicinal chemistry letters, 21(14), 4281-4283 (2011-06-15)
A novel and robust synthesis of the fragment, 2-amino-5-tert-butylpyridine, has been described, which has been shown to have improved physicochemical properties over 4-tert-butylaniline, when considering drug-like properties. The synthesis also yields fragments containing more highly oxidised precursors to the tert-butyl
Novel aromatic polyamides and polyimides functionalized with 4-tert-butyltriphenylamine groups.
Hsiao S-H, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(15), 4579-4592 (2006)
Monica Brivio et al.
Lab on a chip, 5(4), 378-381 (2005-03-26)
The integration of a monitoring port along the microfluidic path of a MALDI-chip integrated device is described. Optimization of the microreactor design allows longer reaction and measuring times. The Schiff base reaction between 4-tert-butylaniline (1) and 4-tert-butylbenzaldehyde (2) in ethanol
Ji Han Kim et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(38), 9060-9070 (2019-04-16)
Organic light-emitting diodes are currently under research to achieve high efficiency and long life by using thermally activated delayed fluorescence (TADF) materials. In particular, many studies have focused on ensuring high efficiency in fluorescent devices by introducing TADF materials. Herein
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