1007375-07-6

Basic information

• Product Name: 1-bromo-3-tert-butyl-2-methoxybenzene
• CAS NO: 1007375-07-6
• Molecular Weight: 243.143
• Mol File: 1007375-07-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-bromo-3-tert-butyl-2-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-3-tert-butyl-2-methoxybenzene(1007375-07-6)
• EPA Substance Registry System: 1-bromo-3-tert-butyl-2-methoxybenzene(1007375-07-6)

Safety Data

• Hazardous Substances Data: 1007375-07-6(Hazardous Substances Data)

Usage

Physical state

Colorless to pale yellow liquid

Odor

Faint aromatic

Usage

Building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Industry application

Pharmaceutical industry for the production of various medications

Role

Intermediate in the synthesis of organic compounds

Function

Precursor in the preparation of various organic compounds

Additional use

Reagent in organic synthesis

Safety

Handle with caution due to hazardous nature and chemical reactivity

Upstream product

• 88-18-6 2-tert-Butylphenol 
• 23159-87-7 2-bromo-6-(tert-butyl)phenol 
• 74-88-4 methyl iodide 

Downstream Products

• 1443670-14-1 2-tert-butyl-6-(octyltelluro)phenol 
• 1443670-18-5 2-tert-butyl-6-(octyltelluro)anisole 
• 1443670-20-9 2-tert-butyl-4-(octyltelluro)anisole 
• 1619266-33-9 C₁₅H₁₉NO 

Relevant articles and documents

Synthesis, characterization, and reactivity of a d2, Mo(IV) complex supported by a new OCO-trianionic pincer ligand

The new terphenyl pincer precursor 3,3″-di-tert-butyl-1,1′:3′,1″-terphenyl-2,2″-diol (1) is examined for its ability to support early transition metals as a trianionic ligand. Metalation proceeds smoothly at -35 °C with Mo(NMe2)4 to

Synthesis and stereochemical properties of "extended" biphenols bridged by ortho-, meta-, and para-phenylene spacers

A series of isomeric biphenols based on para- (1), meta- (2), and ortho- (3) terphenyl backbones was synthesized. Suzuki cross-coupling methodology was employed for the construction of the terphenyl backbone of their methyl-protected precursors (respectiv