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(4-FLUORO-BENZYL)-[2-(1 H-INDOL-3-YL)-ETHYL]-AMINE is a chemical compound with the molecular formula C17H17FN2. It is a derivative of benzylamine and indole, with a fluorine atom attached to the benzene ring. (4-FLUORO-BENZYL)-[2-(1 H-INDOL-3-YL)-ETHYL]-AMINE may have potential applications in medicinal chemistry, particularly in the development of new drug molecules. The presence of the indole group suggests that it may have biological activity, as many natural and synthetic compounds containing indole are known to have pharmacological effects. Further research and testing would be necessary to determine the specific properties and potential uses of this chemical compound.
Used in Pharmaceutical Industry:
(4-FLUORO-BENZYL)-[2-(1 H-INDOL-3-YL)-ETHYL]-AMINE is used as a potential drug molecule for its possible biological activity due to the presence of the indole group. (4-FLUORO-BENZYL)-[2-(1 H-INDOL-3-YL)-ETHYL]-AMINE may be further developed and tested for its pharmacological effects, making it a promising candidate for the creation of new medications.

51841-40-8

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51841-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51841-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51841-40:
(7*5)+(6*1)+(5*8)+(4*4)+(3*1)+(2*4)+(1*0)=108
108 % 10 = 8
So 51841-40-8 is a valid CAS Registry Number.

51841-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(4-fluorophenyl)methyl]-2-(1H-indol-3-yl)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 -
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More Details:51841-40-8 SDS

51841-40-8Downstream Products

51841-40-8Relevant academic research and scientific papers

Indole derivatives with antimycobacterial activity

Mahboobi,Grothus,Meindl

, p. 105 - 114 (2007/10/02)

1,3-Dinitro-2-(indol-3'-yl)-propanes 3 are synthesized by Michael reaction of nitromethane with the indolylnitroethenes 2. - Reaction of the aldehydes 4 and 10 with the benzylamines 12 as well as the reaction of the indolylalkylamines 6a and 9a with the benzaldehydes 11 lead to Schiff bases which are reduced to N-benzyl-(indol-3-ylmethyl)-amines 13 and N-benzyl-(indol-3-ylethyl)-amines 14, respectively; tert amines 16 are synthesized via the formamides 15, amines 18 are prepared according to Mannich. - Inhibitory effects on Mycobacterium tuberculosis H 37 Ra are investigated, a structure-activity relationship is discussed.

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