37796-78-4

Usage

Uses

2-Bromo-6-methylnaphthalene is used in the biosynthesis of penicillin.

Upstream product

• 13720-06-4 2,6-dibromonaphthalene 
• 74-88-4 methyl iodide 
• 15231-91-1 6-bromo-naphthalen-2-ol 
• 13061-96-6 dihydroxy-methyl-borane 
• 151600-02-1 6-bromo-2-naphthalenyl trifluoromethanesulfonate 
• 75-16-1 methylmagnesium bromide 
• 91-57-6 2-Methylnaphthalene 
• 37796-79-5 6-methylnaphthalen-2-amine 

Downstream Products

• 91-57-6 2-Methylnaphthalene 
• 5773-80-8 6-bromo-2-naphthoic acid 
• 1015255-96-5 7-bromo-3-methyl-1-(2,4,6-trimethylphenyl)naphthalene 
• 29304-66-3 2-methyl-6-phenylnaphthalene 
• 32721-06-5 2-(6-bromonaphthalen-2-yl)acetic acid 
• 305798-02-1 2-bromo-6-(bromomethyl)naphthalene 

Relevant academic research and scientific papers

The organic metal compound comprises an organic light emitting element and, and electronic device

An organometallic compound represented by Formula 1:wherein, in Formula 1, R37 is hydrogen, deuterium, a substituted or unsubstituted C1-C60 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C2-C10 heterocycloalkyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C2-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, or a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group; and ring CY1, R21 to R26, R30a, and R30b, are as described herein.

ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME, AND ELECTRONIC APPARATUS INCLUDING THE ORGANIC LIGHT-EMITTING DEVICE

An organometallic compound represented by Formula 1: wherein, in Formula 1, R37 is hydrogen, deuterium, a substituted or unsubstituted C1-C60 alkyl group, a substituted or unsubstituted C3-C10 cycloalkyl group, a substituted or unsubstituted C2-C10 heterocycloalkyl group, a substituted or unsubstituted C6-C60 aryl group, a substituted or unsubstituted C2-C60 heteroaryl group, a substituted or unsubstituted monovalent non-aromatic condensed polycyclic group, or a substituted or unsubstituted monovalent non-aromatic condensed heteropolycyclic group; and ring CY1, R21 to R26, R30a, and R30b, are as described herein.

CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

An organic light-emitting device includes a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode, the organic layer including an emission layer and a condensed cyclic compound of Formula 1. The emi

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

An aromatic amine derivative having ring structures on the both sides of central double bond structure, an organic electroluminescence device including the aromatic amine derivative, and an organic electroluminescence material-containing solution including the aromatic amine derivative as one of organic electroluminescence materials and a solvent, the organic electroluminescence device having a long lifetime and high luminous efficiency and being capable of emitting blue light having a high color purity, and being realized with the aromatic amine derivative and the organic electroluminescence material-containing solution.

Convenient synthesis of 1,1'-binaphthyl-2,2'-dicarboxylic acid

Two syntheses of 1,1'-binaphthyl-2,2'-dicarboxylic acid (4) in good yields are presented via the oxidation of the 2'-methyl substituent of isopropyl 2'-methyl-1,1'-binaphthyl-2-carboxylate (8), which is readily obtainable by the reaction of 2-methyl-1-naphthyl Grignard reagent 7 with isopropyl 1-isopropoxy-2-naphthoate (6).