62498-73-1

Usage

General Description

2-[(butylamino)methyl]phenol is a chemical compound with the formula C11H17NO. It is an organic compound with properties of both an amine and a phenol, containing a butylamine group attached to a phenol ring. It is commonly used as a corrosion inhibitor in various industrial applications, and also as a fragrance ingredient in perfumes and cosmetics. It has been found to possess antimicrobial and antifungal properties, making it useful in the formulation of personal care products and disinfectants. However, it is important to handle this chemical with care, as it can cause skin irritation and may be harmful if swallowed or inhaled.

Upstream product

• 50-00-0 formaldehyd 
• 109-73-9 N-butylamine 
• 108-95-2 phenol 
• 90-02-8 salicylaldehyde 
• 2565-54-0 N-salicylidene-butylamine 
• 144222-43-5 2-Iodo-4,5-dimethoxy-benzoic acid 2-(2-iodo-3-nitro-benzoyloxy)-benzyl ester 
• 90-01-7 salicylic alcohol 
• 144222-47-9 C₂₃H₁₇NO₈ 

Relevant academic research and scientific papers

Anagostic, mono- and hexahapta interactions in Tl(I) dithiocarbamates: A new precursor for the preparation of Tl2S nanoparticles

Two new homoleptic complexes, [Tl(bzfdtc)]2 (1) and [Tl(bu2-OHbzdtc)]2 (2) (where bzfdtc = N-benzyl-N-furfuryldithiocarbamate and bu2-OHbzdtc = (N-butyl-N-(2-hydroxybenzyl)dithiocarbamate), have been prepared an

Carbon dioxide as a carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas: Scope and limitations

Carbon dioxide can be used as a convenient carbonylating agent in the synthesis of 2-oxazolidinones, 2-oxazinones, and cyclic ureas. The transient carbamate anion generated by treating a primary or secondary amine group in basic media can be activated with phosphorylating agents such as Diphenylphosphoryl azide (DPPA) and Diphenyl chlorophosphate (DPPCl) but also with other types of electrophiles such as SOCl2, TsCl, or AcCl. The intramolecular trapping of the activated carbamate by a hydroxyl group leads to the formation of 2-oxazolidinones or 2-oxazinones in good to excellent yields. This methodology was successfully applied to the synthesis of cyclic ureas up to 7-membered rings from the corresponding diamines.

A reductive amination of carbonyls with amines using decaborane in methanol

Aldehydes and ketones were easily converted to the corresponding amines by the reaction of amines in methanol using decaborane (B10H14) at room temperature under nitrogen. The reaction is simple and efficient. The Royal Society of Chemistry 2000.

An Efficient Synthesis of Highly Functionalized Unsymmetrical Biphenyls Having Substituents on the Ortho Positions

The highly functionalized unsymmetrical biphenyls having electron-donating and/or electron-withdrawing substituents on the ortho positions were effectively synthesized based on the intramolecular Ullmann coupling reaction directed by salicyl alcohol as a