Basic information Uses Safety Supplier Related

N,N,2-trimethylquinolin-6-amine

Basic information Uses Safety Supplier Related

N,N,2-trimethylquinolin-6-amine Basic information

Product Name:
N,N,2-trimethylquinolin-6-amine
Synonyms:
  • N,N,2-trimethylquinolin-6-amine
  • N,N,2-Trimethyl-6-quinolinamine
  • 6-Dimethylamino-2-methylquinoline
  • 6-Quinolinamine, N,N,2-trimethyl-
  • N,N,2-trimethylquinolin-6-amine ISO 9001:2015 REACH
  • 6-DIMETILAMINOQUINALDINE
  • 6-DIMETHYLAMINOQUINALDINEM
  • 6 Dimethylamino quinaldin
CAS:
92-99-9
MF:
C12H14N2
MW:
186.25
EINECS:
202-207-3
Product Categories:
  • Quinoline series
Mol File:
92-99-9.mol
More
Less

N,N,2-trimethylquinolin-6-amine Chemical Properties

Melting point:
101°C
Boiling point:
310.75°C (rough estimate)
Density 
1.0859 (rough estimate)
refractive index 
1.6648 (estimate)
storage temp. 
Sealed in dry,Room Temperature
pka
6.58±0.43(Predicted)
Appearance
Light yellow to yellow Solid
EPA Substance Registry System
6-Quinolinamine, N,N,2-trimethyl- (92-99-9)
More
Less

Safety Information

HS Code 
2933499090
More
Less

N,N,2-trimethylquinolin-6-amine Usage And Synthesis

Uses

N,N,2-Trimethylquinoline-6-amine is used as a research compound and in organic synthesis, etc.

Synthesis

123-73-9

99-98-9

92-99-9

4-Amino-N,N-dimethylaniline (10.00 g, 73.4 mmol, source: Alfa Aesar) was dissolved in 6 M aqueous hydrochloric acid solution (132 mL). To this solution was added (E)-2-butenal (10.30 g, 147 mmol, source: Acros) and the mixture was stirred at room temperature for 1 hour. Toluene (70 mL) was then added and the reaction mixture was heated to reflux overnight. Upon completion of the reaction, it was cooled to room temperature, and the organic layer was separated and discarded. The aqueous layer was neutralized with 10% sodium hydroxide solution (350 mL) and subsequently extracted with dichloromethane (2 x 100 mL). The organic phases were combined, washed sequentially with water (2 x 100 mL) and saturated aqueous sodium chloride solution (2 x 100 mL), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Purification by silica gel column chromatography (eluent: ethyl acetate) afforded N,N,2-trimethylquinolin-6-amine 8.44 g (62% yield) as brown solid.1H NMR (500 MHz): δ 7.87 (d, J = 9.3 Hz, 1H), 7.83 (d, J = 8.3 Hz, 1H), 7.31 (dd, J = 9.3, 2.9 Hz, 1H), 7.13 (dd, J = 9.3, 2.9 Hz, 1H), 7.13 (dd, J = 9.3, 2.9 Hz, 1H). 1H), 7.13 (d, J = 8.3 Hz, 1H), 6.76 (d, J = 2.9 Hz, 1H), 3.01 (s, 6H), 2.66 (s, 3H). 13C NMR (125.8 MHz): δ 154.54, 148.12, 141.89, 134.43, 129.10, 127.77, 122.11, 119.30, 105.41, 40.78, 24.92.

References

[1] Organic Letters, 2012, vol. 14, # 24, p. 6366 - 6369
[2] Patent: WO2014/187874, 2014, A1. Location in patent: Page/Page column 25
[3] Patent: CN105018072, 2017, B. Location in patent: Paragraph 0021; 0030; 0031
[4] Patent: CN105001160, 2017, B. Location in patent: Paragraph 0025; 0026; 0027

N,N,2-trimethylquinolin-6-amineSupplier

Shanghai Jian Chao Chemical Technology Co., Ltd.
Tel
150-2103-5486 18017383231
Email
983544897@qq.com
Shanghai Run-Biotech Co., Ltd.
Tel
021-57171705 13817537615
Email
sales@run-biotech.com
Shanghai Hao Yun Chemical Science Co.,Ltd.
Tel
021-68367562 15002147577;
Email
sales@haoyunchem.com
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Email
product02@bidepharm.com
ShangHai D&B Biological Science and Technology Co.Ltd
Tel
400-008-9730,021-54359730 400-008-9730
Email
info@chemxyz.com