51339-31-2

Basic information

• Product Name: (3,5-dibromophenyl)(phenyl)methanol
• Synonyms: (3,5-dibromophenyl)(phenyl)methanol
• CAS NO: 51339-31-2
• Molecular Weight: 342.03
• Mol File: 51339-31-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (3,5-dibromophenyl)(phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-dibromophenyl)(phenyl)methanol(51339-31-2)
• EPA Substance Registry System: (3,5-dibromophenyl)(phenyl)methanol(51339-31-2)

Safety Data

• Hazardous Substances Data: 51339-31-2(Hazardous Substances Data)

Usage

General Description

(3,5-dibromophenyl)(phenyl)methanol is a chemical compound with the molecular formula C13H10Br2O. It is a white to off-white solid and is used in various synthetic and medicinal applications. The compound is a versatile building block in organic synthesis and can be used in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. It is also used as an intermediate in the manufacture of dyes, pigments, and other specialty chemicals. Additionally, (3,5-dibromophenyl)(phenyl)methanol has potential applications in the field of medicinal chemistry, as it exhibits interesting biological activities and pharmacological properties. However, due to its halogenated nature, it is important to handle this compound with care and to adhere to proper safety precautions when working with it.

Upstream product

• 1611-92-3 3,5-dibromotoluene 
• 56990-02-4 3,5-dibromobenzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 56908-88-4 3,5-dibromobenzyl bromide 
• 626-39-1 1,3,5-trisbromobenzene 
• 608-21-9 1,2,3-tribromobenzene 
• 71-43-2 benzene 
• 1137-41-3 (4-aminophenyl)(phenyl)methanone 
• 26733-18-6 4-amino-3,5-dibromo-benzophenone 
• 51339-41-4 (3,5-dibromophenyl)(phenyl)methanone 
• 100-52-7 benzaldehyde 

Downstream Products

• 51339-41-4 (3,5-dibromophenyl)(phenyl)methanone 
• 317334-68-2 1-{3-benzyl-5-[6-(2-morpholin-4-yl-ethylamino)-pyrazin-2-yl]-phenyl}-ethanone 
• 317334-71-7 3-benzyl-5-(5-methylpyrazin-2-yl)methylacetophenone 
• 317334-62-6 3-benzyl-5-(2-oxo-2H-pyridin-1-ylmethyl)acetophenone 
• 317334-67-1 1-[3-benzyl-5-(6-bromo-pyrazin-2-yl)-phenyl]-ethanone 
• 251966-69-5 3-Benzyl-5-1-pyrazin-2-ylmethylacetophenone 
• 317334-94-4 3-benzyl-5-[1,2,4]triazol-1-ylmethylacetophenone 
• 317334-65-9 2-(3-benzyl-5-bromo-phenyl)-2-methyl-[1,3]dioxolane 
• 317332-80-2 1-[3-benzyl-5-(2-oxo-2H-pyridin-1-ylmethyl)phenyl]-3-(4-methylpyridin-2-yl)-propane-1,3-dione 
• 317332-32-4 1-(3-benzyl-5-pyrazin-2-ylmethylphenyl)-3-(4-methylpyridin-2-yl)-propane-1,3-dione 
• 317333-21-4 1-(3-benzyl-5-[1,2,4]triazol-1-ylmethylphenyl)-3-(4-methylpyridin-2-yl)-propane-1,3-dione 
• 214406-54-9 (E)-3-[3-((E)-2-Ethoxycarbonyl-vinyl)-5-(hydroxy-phenyl-methyl)-phenyl]-acrylic acid ethyl ester 
• 422550-95-6 3-[({2-[3-benzyl-5-(1,1-dioxo-isothiazolidin-2-ylmethyl)-phenyl]-2-oxo-ethyl}-benzyloxycarbonyl-amino)-methyl]-pyridine-2-carboxylic acid ethyl ester 
• 1026627-33-7 {2-[3-benzyl-5-(1,1-dioxo-isothiazolidin-2-ylmethyl)-phenyl]-2-oxo-ethyl}-(2-chloro-pyridin-3-ylmethyl)-carbamic acid benzyl ester 

Relevant articles and documents

Preparation and application of organic thermally induced delayed fluorescence material containing 9,9-dimethyl acridine unit

The invention belongs to the field of organic luminescent materials, and provides preparation and application of an organic thermally induced delayed fluorescence material containing a 9,9-dimethyl acridine unit. Isophthalonitrile with high eletrophilicity is taken as the electron acceptor, a cyano group with a strong electron-withdrawing performance is introduced, 9,9-dimethyl acridine is taken as the electron donor, and a meta-position connection mode is adopted to obtain the organic micromolecular thermally induced delayed fluorescence material with an excellent luminescence property, and the conventional para-position connection mode is broken through. The organic thermally induced delayed fluorescence material, which contains a 9,9-dimethyl acridine unit and adopts a meta-position connection mode, can be applied to vapor deposition of devices. Meanwhile, the organic thermally induced delayed fluorescence material has the advantages of high yield, high thermal stability, and easy film forming, can be massively produced and used in a large scale, and can be applied to electroluminescent devices to obtain a high efficient electroluminescent performance.

Design and synthesis of 8-hydroxy-[1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells

Naphthyridine 7 inhibits the strand transfer of the integration process catalyzed by integrase with an IC50 of 10 nM and inhibits 95% of the spread of HIV-1 infection in cell culture at 0.39 μM. It does not exhibit cytotoxicity in cell culture

HIV integrase inhibitors

Certain six-membered aromatic and heteroaromatic-dioxobutyric acid derivatives are described as inhibitors of HIV integrase and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HIV and the treatment