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355381-83-8

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355381-83-8 Usage

Description

(3,4-DIMETHOXY-BENZYL)-[2-(4-FLUORO-PHENYL)-ETHYL]-AMINE is a complex organic compound that features a benzyl group with two dimethoxy substituents and an amine group attached to a 2-(4-fluoro-phenyl)ethyl group. This molecule contains aromatic rings and amine functional groups, which may confer properties akin to other compounds with similar chemical structures. Its unique structural and electronic characteristics suggest potential applications in pharmaceutical research, organic synthesis, and various industrial fields.

Uses

Used in Pharmaceutical Research:
(3,4-DIMETHOXY-BENZYL)-[2-(4-FLUORO-PHENYL)-ETHYL]-AMINE is used as a chemical intermediate for the development of new pharmaceuticals, leveraging its structural and electronic properties to create novel drug candidates.
Used in Organic Synthesis:
In the field of organic synthesis, (3,4-DIMETHOXY-BENZYL)-[2-(4-FLUORO-PHENYL)-ETHYL]-AMINE serves as a building block or reactant in the synthesis of more complex organic molecules, contributing to the creation of advanced materials and specialty chemicals.
Used in Industrial Applications:
(3,4-DIMETHOXY-BENZYL)-[2-(4-FLUORO-PHENYL)-ETHYL]-AMINE is utilized in various industrial applications, potentially including the development of new materials, chemical processes, or as a component in formulations that require its specific chemical attributes.

Check Digit Verification of cas no

The CAS Registry Mumber 355381-83-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,3,8 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 355381-83:
(8*3)+(7*5)+(6*5)+(5*3)+(4*8)+(3*1)+(2*8)+(1*3)=158
158 % 10 = 8
So 355381-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H20FNO2/c1-20-16-8-5-14(11-17(16)21-2)12-19-10-9-13-3-6-15(18)7-4-13/h3-8,11,19H,9-10,12H2,1-2H3

355381-83-8SDS

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 N-[(3,4-dimethoxyphenyl)methyl]-2-(4-fluorophenyl)ethanamine

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:355381-83-8 SDS

355381-83-8Downstream Products

355381-83-8Relevant articles and documents

Synthesis, structure-activity relationship and in vitro biological evaluation of N-arylethyl isoquinoline derivatives as Coxsackievirus B3 inhibitors

Wang, Yan-Xiang,Li, Yu-Huan,Li, Ying-Hong,Gao, Rong-Mei,Wang, Hui-Qiang,Liu, Yan-Xin,Gao, Li-Mei,Lu, Qiao-Ni,Jiang, Jian-Dong,Song, Dan-Qing

, p. 5787 - 5790 (2011/10/18)

Currently, there is no approved antiviral drug for the infection caused by enteroviruses. A series of novel N-arylethyl isoquinoline derivatives defined with substituents on the ring A and C were designed, synthesized and evaluated in vitro for their activities against Coxsackievirus B3 (CVB3). The primary structure-activity relationship revealed that substituents on the ring A were not beneficial for the activity. Among these analogs synthesized, compound 7f bearing a methylenedioxy at the R4 and R5 positions afforded an anti-CVB3 activity and a reasonable selectivity index (SI = 26.8); furthermore, 7f exhibited a moderate activity against enterovirus 71 (EV71) with SI value of 9.0. Thus it has been selected as an anti-enteroviral lead compound for further investigation.

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