6839-10-7

Basic information

• Product Name: 1-Naphthalenemethanol, a-(2-methoxyphenyl)-
• CAS NO: 6839-10-7
• Molecular Formula: C18H16O2
• Molecular Weight: 264.324
• Mol File: 6839-10-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenemethanol, a-(2-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenemethanol, a-(2-methoxyphenyl)-(6839-10-7)
• EPA Substance Registry System: 1-Naphthalenemethanol, a-(2-methoxyphenyl)-(6839-10-7)

Safety Data

• Hazardous Substances Data: 6839-10-7(Hazardous Substances Data)

Usage

Physical state

White solid

Aroma

Floral, sweet

Common uses

Production of perfumes, soaps, and cosmetics

Additional uses

Fragrance in personal care products, flavoring agent in the food industry

Toxicity

Low toxicity, generally considered safe for use in consumer products when used as directed

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 703-55-9 1-naphthylmagnesiumbromide 
• 13922-41-3 1-Naphthylboronic acid 
• 18052-80-7 1-naphthyltrimethylsilane 

Downstream Products

• 6839-17-4 bis-[(2-methoxy-phenyl)-[1]naphthyl-methyl]-ether 

Relevant articles and documents

Bis(2-alkylpyrrolidin-1-yl)methylidenes as chiral acyclic diaminocarbene ligands

2-Alkylpyrrolidines were used as building blocks for acyclic diaminocarbenes (ADCs). First, ureas were made from the corresponding amines, and then the ureas were converted to chloroamidiniums. The chloroamidiniums served as direct precursors to ADCs, and

Phosphazene base-promoted functionalization of aryltrimethylsilanes

The activation of Ar-Si bonds in aryltrimethylsilane was investigated using a catalytic amount of t-Bu-P4 base and selective functionalizations of aryltrimethylsilanes in the absence of strong electron withdrawing groups on the aromatic rings were accomplished. The Royal Society of Chemistry 2006.