23450-18-2

Basic information

• Product Name: 2-BROMODIPHENYLMETHANE
• Synonyms: 2-BROMODIPHENYLMETHANE
• CAS NO: 23450-18-2
• Molecular Formula: C₁₃H₁₁Br
• Molecular Weight: 247.13
• Mol File: 23450-18-2.mol
• Article Data: 35

Chemical Properties

• Boiling Point: 109 °C
• Flash Point: 140.9 °C
• Appearance: /
• Density: 1.34
• CAS DataBase Reference: 2-BROMODIPHENYLMETHANE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMODIPHENYLMETHANE(23450-18-2)
• EPA Substance Registry System: 2-BROMODIPHENYLMETHANE(23450-18-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 23450-18-2(Hazardous Substances Data)

Usage

General Description

2-Bromodiphenylmethane is an organic compound with the chemical formula C13H11Br. It is a colorless to light yellow liquid that is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2-Bromodiphenylmethane is also used as a reactant in the production of dyes and pigments. It is a brominated derivative of diphenylmethane, and its chemical structure makes it useful in various chemical reactions and organic synthesis processes. Due to its reactivity and potential hazards, 2-Bromodiphenylmethane should be handled and stored with proper safety precautions according to standard chemical handling and storage guidelines.

Upstream product

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Downstream Products

• 740-35-2 2'-Fluor-2-benzyl-benzophenon 
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Relevant articles and documents

A novel spiro-functionalized polyfluorene derivative with solubilizing side chains

We report on a new polyfluorene derivative containing a spiroanthracenefluorene unit with a remote C-10 position that provides facile substitution of alkyl groups. An ethylhexyl group was introduced into the spiroanthracenefluorene unit and the ethylhexyl

STEREORETENTIVE CROSS-COUPLING OF BORONIC ACIDS

The present disclosure provides tri-orthoalkylphenyl phosphine catalysts that are tuned electrically and sterically. Method of using the catalyst for cross-coupling of unactivated secondary boronic acids with near-perfect levels of site- and stereoretention are also provided.

Synthetic method of diarylmethanes

The invention discloses a synthetic method of diarylmethanes. The method is characterized in that benzyl pseudohalide and aromatic boric acid are reacted in an organic solvent under alkaline condition. The method employs easily available raw materials, conversion is realized under effect of no transition metal catalysis, water-free and oxygen-free are not required, Lewis acid catalysis is not required, the method has wide substrate universality, and various substituted diarylmethanes can be synthesized by the method.