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Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(4-Methoxy-1-phenylnaphthalen-2-yl)Methanol is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its role in these industries is crucial for the development of new drugs and agricultural products, contributing to advancements in healthcare and agriculture.
Used in Organic Chemicals Production:
(4-Methoxy-1-phenylnaphthalen-2-yl)Methanol is also employed in the production of organic chemicals, where it serves as a key component in the creation of a range of chemical products. Its presence in this sector highlights the importance of (4-Methoxy-1-phenylnaphthalen-2-yl)Methanol in the broader chemical industry.
Used in Fragrance Industry:
(4-Methoxy-1-phenylnaphthalen-2-yl)Methanol is used as a fragrance ingredient in the perfume and cosmetic products industry. Its incorporation into these products enhances their scent profiles, providing consumers with a diverse array of olfactory experiences.
Used in Organic Electronics and Materials Science:
Furthermore, (4-Methoxy-1-phenylnaphthalen-2-yl)Methanol has potential applications in the field of organic electronics and materials science. Its unique properties make it a promising candidate for research and development in these cutting-edge areas.
Precaution:
It is essential to handle (4-Methoxy-1-phenylnaphthalen-2-yl)Methanol with care, as it can pose health and environmental risks if not used properly. Safe handling protocols and proper disposal methods should be followed to minimize any potential hazards associated with (4-Methoxy-1-phenylnaphthalen-2-yl)Methanol.

Upstream product

• 78250-30-3 Methyl 4-methoxy-1-phenyl-2-naphthoate 
• 78250-28-9 ethyl 4-acetoxy-1-phenyl-2-naphthoate 
• 78250-29-0 Methyl 4-hydroxy-1-phenyl-2-naphthoate 
• 78250-27-8 1-phenyl-4-hydroxy-2-naphthoic acid 
• 345307-72-4 Acetic acid 4-methoxy-1-phenyl-naphthalen-2-ylmethyl ester 

Downstream Products

• 345307-72-4 Acetic acid 4-methoxy-1-phenyl-naphthalen-2-ylmethyl ester 
• 78250-35-8 1-Phenyl-2-(N-benzyl,N',N'-dibenzylpiperazinomethyl)-4-<β-(N-benzyl-N,N-dimethyl)aminoethoxy>naphthalene tribromid 
• 78250-14-3 (4-methoxy-1-phenyl-naphth-2-ylmethyl)(β-phenoxyethyl)diethylammonium bromide 
• 78266-24-7 (4-methoxy-1-phenyl-naphth-2-ylmethyl)(β-phenoxyethyl)dimethylammonium bromide 
• 78250-11-0 4-methoxy-1-phenyl-2-(4'-(o-tolyl)piperazino)naphthalene 
• 78250-12-1 4-methoxy-1-phenyl-2-(4'-carbethoxypiperazino)naphthalene 
• 78250-09-6 4-methoxy-1-phenyl-2-(4'-benzylpiperazino)naphthalene 
• 78250-10-9 4-methoxy-1-phenyl-2-(4'-phenylpiperazino)naphthalene 
• 78250-36-9 3-(4-Benzyl-piperazin-1-ylmethyl)-4-phenyl-naphthalen-1-ol 
• 78250-08-5 4-methoxy-1-phenyl-2-(4'-methylpiperazino)naphthalene 
• 78250-33-6 2-Bromomethyl-4-methoxy-1-phenylnaphthalene 

Relevant academic research and scientific papers

Syntheses of 2,4-Disubstituted 1-Phenylnaphthalenes 5-Substituted Benzofluoren-7(H)-ones as Possible Anti-hookworm Agents

Various 2,4-disubstituted 1-phenylnaphthalenes and 5-substituted benzofluoren-7(H)-ones have been synthesised and evaluated for their anti-hookworm activity against N. brasiliensis in rats.The compounds do not show any significant activity.During the reac

Acylation of Alcohols by Fatty Acid Esters in Presence of Lithium Aluminium Hydride

A novel acylation of alcohols by fatty acid esters in the presence of lithium aluminium hydride is reported.A plausible mechanism of this acylation through the formation of a lithium aluminium tetraalkoxide complex has been suggested.