211734-49-5

Basic information

• Product Name: (R)-3,3'-Dibromo-2,2'-bis(meth
• Synonyms: (R)-3,3'-Dibromo-2,2'-bis(meth;(R)-3,3'-Dibromo-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl, 97%;(R)-3,3'-Dibromo-bis(methoxymethoxyl)-1,1'-binaphtyl, 99%e.e.
• CAS NO: 211734-49-5
• Molecular Formula: C₂₄H₂₀Br₂O₄
• Molecular Weight: 532.22
• Mol File: 211734-49-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (R)-3,3'-Dibromo-2,2'-bis(meth(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3,3'-Dibromo-2,2'-bis(meth(211734-49-5)
• EPA Substance Registry System: (R)-3,3'-Dibromo-2,2'-bis(meth(211734-49-5)

Safety Data

• Hazardous Substances Data: 211734-49-5(Hazardous Substances Data)

Usage

General Description

(R)-3,3'-Dibromo-2,2'-bis(methylpropyl)-5,5'-dimethylbiphenyl is a chemical compound consisting of a central biphenyl core with methylpropyl and bromine substituents. It has a chiral structure with a specific spatial orientation, denoted by the (R) designation. (R)-3,3'-Dibromo-2,2'-bis(meth is commonly used in organic synthesis and materials science, particularly as a building block for the preparation of liquid crystals and other functional materials. Its unique structure and properties make it a valuable component in the development of advanced materials for various industrial applications. The presence of bromine substituents also gives this compound potential for use in pharmaceuticals and agrochemicals, where halogen atoms can impart useful properties to the molecules.

Upstream product

• 173831-50-0 rac-2,2'-bis-(methoxymethoxy)-1,1'-binaphthalene 
• 135-19-3 β-naphthol 
• 602-09-5 1,1'-bi-2-naphthol 

Downstream Products

• 756491-45-9 (+/-)-3,3'-bis(4-methoxyphenyl)-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl 
• 756491-46-0 (+/-)-3,3'-bis(3,5-dimethylphenyl)-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl 
• 1621066-21-4 3,3'-bis(4-(trifluoromethyl)phenyl)-[1,1'-binaphthalene]-2,2'-diol 
• 263165-80-6 3,3'-Bis-(2-methoxy-phenyl)-[1,1']binaphthalenyl-2,2'-diol 
• 215433-51-5 (+/-)-3,3'-bis(3,5-dimethylphenyl)-2,2'-dihydroxy-1,1'-binaphthyl 
• 1199631-29-2 (+/-)-3,3'-bis(4-methoxyphenyl)-2,2'-dihydroxy-1,1'-binaphthyl 
• 75640-70-9 3,3'-diphenyl-1,1'-bi-2-naphthol 
• 428874-67-3 (±)?3,3'?diphenyl?2,2'?bis(methoxymethyl)?1,1'?binaphthalene 
• 211734-50-8 2,2'-Bis-methoxymethoxy-3,3'-bis-(2-methoxy-phenyl)-[1,1']binaphthalenyl 

Relevant articles and documents

Synthesis of (±)-3,3′-diphenyl-2,2′-binaphthol via different routes using Pd and Ni as catalyst respectively

3,3′-Biphenyl-2,2′-binaphthols (BINOLs) are precursors of phosphoric acids that are widely used as ligands and catalysts in organic reactions. In this report, two routes for the synthesis of (±)-3,3′-diphenyl BINOLs via (±)-3,3′ bis-halogenated BINOLs int

Synthesis, properties, and structures of functionalized peri -xanthenoxanthene

Three types of alkylated peri-xanthenoxanthene (PXX) have been synthesized employing efficient synthetic routes. These heteroaromatic compounds exhibited different electronic and crystal structures according to UV-vis spectra, electrochemical measurements, and X-ray structural analyses. Among them, 1,7-DOPXX has been demonstrated as an active material for organic field-effect transistors with promising mobility and a high on/off ratio simultaneously.