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(2-fluoro-benzyl)-(3-morpholin-4-yl-propyl)-amine is a chemical compound that features a fluoro-benzyl group attached to a morpholin-4-yl-propylamine moiety. (2-fluoro-benzyl)-(3-morpholin-4-yl-propyl)-amine is known for its unique chemical properties and potential therapeutic applications.

247907-33-1

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247907-33-1 Usage

Uses

Used in Pharmaceutical Research:
(2-fluoro-benzyl)-(3-morpholin-4-yl-propyl)-amine is used as a therapeutic agent in pharmaceutical research for its potential to enhance drug binding to specific targets in the body. The fluoro-benzyl group contributes to its unique chemical properties, while the morpholin-4-yl-propylamine moiety, a common structural feature in many biologically active compounds, is known for its ability to modulate receptor activity. This makes (2-fluoro-benzyl)-(3-morpholin-4-yl-propyl)-amine a valuable component in drug discovery and development efforts.

Check Digit Verification of cas no

The CAS Registry Mumber 247907-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,9,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 247907-33:
(8*2)+(7*4)+(6*7)+(5*9)+(4*0)+(3*7)+(2*3)+(1*3)=161
161 % 10 = 1
So 247907-33-1 is a valid CAS Registry Number.

247907-33-1Upstream product

247907-33-1Downstream Products

247907-33-1Relevant academic research and scientific papers

A mild chemospecific reductive dehalogenation of ethylaminobenzamides with lithium aluminum hydride

Hendrix, James A.,Stefany, David W.

, p. 6749 - 6752 (2007/10/03)

A mild reduction of ortho-fluoro benzamides was discovered using LAH. The reaction proceeds cleanly and in moderate yields. The scope of the reaction is explored and a mechanism is proposed. A two carbon spacer between the amide and a 3°amine is optimal for this chelation controlled reaction.

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