1037085-24-7

Basic information

• Product Name: (2-(naphthalen-2-yl)phenyl)methanol
• Synonyms: (2-(naphthalen-2-yl)phenyl)methanol
• CAS NO: 1037085-24-7
• Molecular Weight: 234.298
• Mol File: 1037085-24-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2-(naphthalen-2-yl)phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-(naphthalen-2-yl)phenyl)methanol(1037085-24-7)
• EPA Substance Registry System: (2-(naphthalen-2-yl)phenyl)methanol(1037085-24-7)

Safety Data

• Hazardous Substances Data: 1037085-24-7(Hazardous Substances Data)

Upstream product

• 223575-47-1 2-(naphthalen-2’-yl)benzaldehyde 
• 32316-92-0 naphthalene-2-boronic acid 
• 6630-33-7 ortho-bromobenzaldehyde 
• 5159-41-1 2-iodobenzyl alcohol 

Downstream Products

• 1623102-59-9 2-(2-(prop-2-yn-1-yl)phenyl)naphthalene 
• 154380-69-5 C₁₇H₁₃Br 
• 3697-24-3 5-methylchrysene 
• 1618650-42-2 2-(2-(azidomethyl)phenyl)naphthalene 

Relevant articles and documents

Pd-catalyzed atom-efficient cross-coupling of triarylbismuth reagents with protecting group-free iodophenylmethanols: Synthesis of biarylmethanols

An atom-efficient procedure for the synthesis of functionalized biarylmethanols via the Pd-catalyzed cross-coupling reactions of differently functionalized iodophenylmethanols and triarylbismuth reagents is described. This protecting group-free direct couplings of 2-, 3- or 4-iodophenylmethanols with triarylbismuth reagents afforded biarylmethanols in good to high yields.

A new synthetic approach to 6-unsubstituted phenanthridine and phenanthridine-like compounds under mild and metal-free conditions

A new and mild synthetic approach for the synthesis of 6-unsubstituted phenanthridine and phenanthridine-like compounds under metal-free conditions at room temperature has been developed. The strategy involved a tandem azide rearrangement/intramolecular annulation and oxidation reactions of biarylmethyl azide precursors to obtain the desired products in up to 99% yields with high regioselectivity.

MODULATORS OF C3A RECEPTOR AND METHODS OF USE THEREOF

Provided are compounds that are modulators of C3a receptor activity, compositions containing the compounds and methods of use of the compounds and compositions. In certain embodiments, the compounds are pyridones. In certain embodiments, provided are methods for treatment or amelioration of diseases associated with modulation of C3a receptor activity.