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2,2,2-TRIFLUORO-1-(4-METHOXY-PHENYL)-ETHYLAMINE HYDROCHLORIDE is a white crystalline solid with the molecular formula C9H12F3NO. It is a chemical compound that is widely used in the pharmaceutical industry as an intermediate for the synthesis of various drugs. 2,2,2-TRIFLUORO-1-(4-METHOXY-PHENYL)-ETHYLAMINE HYDROCHLORIDE is known for its reactivity and ability to participate in different chemical reactions, making it a valuable asset in both the pharmaceutical and chemical industries.

65686-77-3

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65686-77-3 Usage

Uses

Used in Pharmaceutical Industry:
2,2,2-TRIFLUORO-1-(4-METHOXY-PHENYL)-ETHYLAMINE HYDROCHLORIDE is used as a key intermediate in the synthesis of various drugs for treating a wide range of conditions, including psychiatric disorders and neurological diseases. Its unique structure and reactivity contribute to the development of effective medications that address these health issues.
Used in Organic Chemistry:
In the field of organic chemistry, 2,2,2-TRIFLUORO-1-(4-METHOXY-PHENYL)-ETHYLAMINE HYDROCHLORIDE is utilized for its reactivity and ability to participate in various chemical reactions. This property makes it a valuable compound for researchers and chemists working on the development of new chemical processes and products.
Used in Research and Industrial Applications:
The hydrochloride form of 2,2,2-TRIFLUORO-1-(4-METHOXY-PHENYL)-ETHYLAMINE HYDROCHLORIDE is commonly used in research and industrial applications due to its stability and ease of handling. Its stable nature allows for more efficient and reliable experimentation, making it a preferred choice for scientists and professionals in the industry.

Check Digit Verification of cas no

The CAS Registry Mumber 65686-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,8 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65686-77:
(7*6)+(6*5)+(5*6)+(4*8)+(3*6)+(2*7)+(1*7)=173
173 % 10 = 3
So 65686-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H10F3NO.ClH/c1-14-7-4-2-6(3-5-7)8(13)9(10,11)12;/h2-5,8H,13H2,1H3;1H

65686-77-3 Well-known Company Product Price

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  • Aldrich

  • (JWP00278)  2,2,2-Trifluoro-1-(4-methoxy-phenyl)-ethylamine hydrochloride  AldrichCPR

  • 65686-77-3

  • JWP00278-1G

  • 7,733.70CNY

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65686-77-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-1-(4-methoxyphenyl)ethanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65686-77-3 SDS

65686-77-3Downstream Products

65686-77-3Relevant academic research and scientific papers

Thermocontrolled benzylimine-benzaldimine rearrangement over Nafion-H catalysts for efficient entry into α-trifluoromethylbenzylamines

Prakash, G.K. Surya,Glinton, Kevin E.,Panja, Chiradeep,Gurung, Laxman,Battamack, Patrice T.,T?r?k, Béla,Mathew, Thomas,Olah, George A.

experimental part, p. 607 - 611 (2012/02/13)

Nafion-H and Nafion SAC-13 are efficient solid Br?nsted acid catalysts for the preparation of trifluoromethyl ketimines from benzylamines and trifluoromethylated ketones in high yields. A finely tuned benzylimine- benzaldimine rearrangement by facile 1,3-hydrogen shift has been achieved for the formation of fluorinated benzaldimines in high yields by careful optimization of reaction conditions including attempts under microwave conditions and a flow system. These α-trifluoromethylated benzaldimines are efficient precursors for pharmaceutically important α- trifluoromethylated benzylamines, accessed through their direct acid hydrolysis.

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