2069-41-2

Basic information

• Product Name: 4-bromo-4'-fluorobenzophenone
• Synonyms: (4-bromophenyl)-(4-fluorophenyl)methanone;Methanone, (4-broMophenyl)(4-fluorophenyl)-
• CAS NO: 2069-41-2
• Molecular Formula: C₁₃H₈BrFO
• Molecular Weight: 279.12
• EINECS: 218-193-7
• Mol File: 2069-41-2.mol
• Article Data: 13

Chemical Properties

• Melting Point: 107-108 °C
• Boiling Point: 353.4±22.0 °C(Predicted)
• Appearance: /
• Density: 1.485±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-bromo-4'-fluorobenzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-4'-fluorobenzophenone(2069-41-2)
• EPA Substance Registry System: 4-bromo-4'-fluorobenzophenone(2069-41-2)

Safety Data

• Hazardous Substances Data: 2069-41-2(Hazardous Substances Data)

Usage

General Description

4-Bromo-4'-fluorobenzophenone is a chemical compound classified as a halogenated benzophenone. It is a white crystalline solid with the molecular formula C13H8BrFO. 4-bromo-4'-fluorobenzophenone is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block in the production of dyes and other organic compounds. 4-Bromo-4'-fluorobenzophenone is known for its high chemical stability and low reactivity, making it a valuable reagent in organic chemistry. It is important to handle this compound with care, as it is hazardous if ingested, inhaled, or comes into contact with skin.

Upstream product

• 108-86-1 bromobenzene 
• 403-43-0 4-fluorobenzoyl chloride 
• 462-06-6 fluorobenzene 
• 586-75-4 4-chlorobenzoyl chloride 
• 106-37-6 1.4-dibromobenzene 
• 116332-54-8 4-fluoro-N-methoxy-N-methylbenzamide 
• 133472-27-2 4-fluorophenylzinc chloride 
• 17100-44-6 4-bromo-4α-fluorodiphenylmethane 
• 586-76-5 4-Bromobenzoic acid 
• 589-17-3 p-bromobenzyl chloride 

Downstream Products

• 3851-47-6 4-bromo-4'-fluorodiphenylmethanol 
• 153354-46-2 4-fluoro-4'-phenylethynylbenzophenone 
• 933037-26-4 1-(4-bromo-phenyl)-1-(4-imidazol-1-yl-phenyl)-methanone 
• 1016749-24-8 (4-bromophenyl)(4-fluorophenyl)methanamine 
• 1428526-90-2 tert-butyl (4-bromophenyl)(4-fluorophenyl)methylcarbamate 
• 1428526-92-4 ethyl 4-(amino(4-fluorophenyl)methyl)phenyl(methyl)phosphinate hydrochloride 
• 1428526-93-5 ethyl 4-((4-fluorophenyl)(4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxamido)methyl)phenyl(methyl)phosphinate 
• 1428526-94-6 4-((4-fluorophenyl)(4-hydroxy-2-(1H-pyrazol-1-yl)pyrimidine-5-carboxamido)methyl)phenyl(methyl)phosphinic acid 
• 1428526-91-3 C₂₁H₂₇FNO₄P 
• 1445534-21-3 C₁₄H₉BrFNO 
• 876301-88-1 (4-bromophenyl)(4-(diphenylamino)phenyl)methanone 

Relevant articles and documents

AIBN initiated functionalization of the benzylic sp3 C[sbnd]H and C[sbnd]C bonds in the presence of dioxygen

A sp3 C[sbnd]H bond functionalization and C[sbnd]C bond cleavage were realized by AIBN/O2 catalyst system, providing a series of benzophenones under mild reaction conditions. The mechanistic study shows that a peroxide intermediate is involved in this transformation, and in the case of diphenylmethanes, the sp3 C[sbnd]C bond is cleaved through the peroxide rearrangement, which might provides a new way to cleave relatively strong C[sbnd]C bond and be applied to more general C[sbnd]C bond activation.

Organic white light material with thermal activation delay and aggregation-induced emission performance and synthetic method and application thereof

The invention provides an organic white light material with the terminal activation delay and aggregation-induced emission performance and a synthetic method and application thereof. The general molecular formula of the white light material is Ar-Ar1-Ar2, wherein Ar is a phenothiazine electron-donating substituent group, Ar1 is a strong electron-withdrawing group, and Ar2 is an aromatic fused ring or heterocyclic aromatic substituent group except phenothiazine. The synthetic method of the material is simple, the thermal performance, luminous efficiency and white light color purity of an end product can be adjusted through connection of different aromatic fused ring or heterocyclic aromatic groups, the white light material has the thermal activation delay and aggregation-induced emission properties, the glass transition temperature is high, and the emission performance is excellent. The obtained white light material is a light emitting layer applied to preparing a non-doped OLED device, the illumination brightness is high, the stability is good, and the practicability requirement can be met.

SUBSTITUTED PYRIMIDINES

The present invention relates to substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.