62498-73-1

Basic information

• Product Name: 2-[(butylamino)methyl]phenol
• Synonyms: 2-[(butylamino)methyl]phenol
• CAS NO: 62498-73-1
• Molecular Formula: C₁₁H₁₇NO
• Molecular Weight: 179.25878
• Mol File: 62498-73-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(butylamino)methyl]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(butylamino)methyl]phenol(62498-73-1)
• EPA Substance Registry System: 2-[(butylamino)methyl]phenol(62498-73-1)

Safety Data

• Hazardous Substances Data: 62498-73-1(Hazardous Substances Data)

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

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

Relevant articles and documents

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

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