ChemicalBook--->CAS DataBase List--->325-14-4

325-14-4

325-14-4 Structure

325-14-4 Structure
IdentificationMore
[Name]

7-(TRIFLUOROMETHYL)QUINOLINE
[CAS]

325-14-4
[Synonyms]

7-(TRIFLUOROMETHYL)QUINOLINE
[Molecular Formula]

C10H6F3N
[MDL Number]

MFCD00833760
[Molecular Weight]

197.16
[MOL File]

325-14-4.mol
Chemical PropertiesBack Directory
[Melting point ]

65-67°C
[Boiling point ]

236.6℃ (762 Torr)
[density ]

1.311±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

2.55±0.14(Predicted)
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

325-14-4(CAS DataBase Reference)
[Storage Precautions]

Store under nitrogen;Moisture sensitive
Safety DataBack Directory
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2933499090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sulfuric acid-->Glycerol-->Sodium iodide-->Oxalic acid-->3-Aminobenzotrifluoride-->3-Nitrobenzotrifluoride-->7-(Trifluoromethyl)-1,2,3,4-tetrahydroquinoline-->4-Chloro-7-(trifluoromethyl)quinoline-->Potassium iodide
[Preparation Products]

(Quinolin-7-yl)methanamin hydrochloride-->7-(Trifluoromethyl)-1,2,3,4-tetrahydroquinoline
Hazard InformationBack Directory
[Chemical Properties]

yellow powder
[Synthesis]

3-Aminobenzotrifluoride

98-16-8

Glycerol

56-81-5

7-(TRIFLUOROMETHYL)QUINOLINE

325-14-4

1. Concentrated sulfuric acid (13.7 g, 0.14 mol) was slowly added dropwise to glycerol (8.63 g, 0.094 mol) at a controlled temperature not exceeding 70 °C. 2. m-Trifluoromethylaniline (5.00 g, 0.031 mol) was added to the above mixture, and the reaction was heated up to 85 °C, and kept at 85 °C for 40 min. 3. Potassium iodide (0.30 g, 1.80 mmol), iodine (0.34 g, 1.34 mmol), and water (1.50 mL) were added in sequence, and the reaction system was heated up to 135 °C for 4 hours. 4. 1.80 mmol), iodine (0.34 g, 1.34 mmol) and water (1.50 mL) were added sequentially, and the reaction system was heated to 135 °C and the reaction was sustained for 4 h. 4. Upon completion of the reaction, it was cooled to room temperature, and the reaction mixture was quenched by pouring it into iced water and filtered through diatomaceous earth. 5. The filtrate was adjusted to a pH of 7 with ammonia, pumped, and the filtrate was extracted with ethyl acetate. 6. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure.7. The residue was purified by column chromatography to afford 7-trifluoromethylquinoline (3.50 g, 69% yield).

[References]

[1] Patent: CN108409649, 2018, A. Location in patent: Paragraph 0042; 0043; 0044
[2] Patent: US2010/234340, 2010, A1. Location in patent: Page/Page column 21
Spectrum DetailBack Directory
[Spectrum Detail]

7-(TRIFLUOROMETHYL)QUINOLINE(325-14-4)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

7-(Trifluoromethyl)quinoline, 97%(325-14-4)
325-14-4 suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Alfa Aesar  
Telephone: 400-6106006
Website: http://chemicals.thermofisher.cn
Company Name: Energy Chemical  
Telephone: 400-0056266
Website: www.energy-chemical.com
Company Name: Capot Chemical Co., Ltd  
Telephone: +86 (0) 571 85 58 67 18
Website: www.capotchem.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Telephone: 021-54306202 13764082696
Website: https://www.hanhongsci.com
Company Name: Chengdu Forest Science and Technology Development Co., Ltd.  
Telephone: 18030648795 18030648795
Website: www.cdforestchem.com
Company Name: Shanghai Run-Biotech Co., Ltd.  
Telephone: 021-57171705 13817537615
Website: www.run-biotech.com
Company Name: Wuxi Zhangkun Biochemical Technology Co., Ltd.  
Telephone: +86 0510-85629785
Website: www.chemicalbook.com/ShowSupplierProductsList16040/0_EN.htm
Company Name: Shanghai Meishui Chemical Technology Co., Ltd  
Telephone: 021-60549325 18616193163
Website: www.chemicalbook.com/ShowSupplierProductsList16215/0_EN.htm
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: Wuxi Zhongkun Biochemical Technology Co., Ltd.  
Telephone: 0510-85629785 18013409632;
Website: www.reading-chemicals.com
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Telephone: 025-66028182 17714375163
Website: www.aikonchem.com
Company Name: Hangzhou Milestone Pharmtech Co., Ltd.  
Telephone: 0571-82896630 18969958410
Website: http://www.milestonepharmtech.cn/
Company Name: Amadis Chemical Company Limited  
Telephone: 571-89925085
Website: http://www.amadischem.com
Company Name: Nanijing m&m biotechnology Co. ,Ltd.  
Telephone: 025-87782433 18021532344
Website: http://www.marymebiotech.com
Company Name: Capot Chemical Co.,Ltd.  
Telephone: +86-(0)57185586718 +86-13336195806
Website: www.capot.com/
Company Name: Tianjin heowns Biochemical Technology Co., Ltd.  
Telephone: 400-6387771-6039 18920764717
Website: www.heowns.com
Company Name: Shanghai Medicil Biomedical Co., Ltd.  
Telephone: 021-50822001
Website: www.chemicalbook.com/ShowSupplierProductsList30881/0_EN.htm
Tags:325-14-4 Related Product Information
71083-18-6 1701-24-2 23779-97-7 346-55-4 83012-13-9 322-97-4 1698-53-9 1701-19-5 18706-21-3 49713-56-6 51773-92-3 450-62-4 49713-51-1 18706-35-9 1701-20-8 574-92-5 23779-96-6 18529-09-4