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

Description

(3,5-dibromophenyl)(phenyl)methanol, with the molecular formula C13H10Br2O, is a white to off-white solid chemical compound. It serves as a versatile building block in organic synthesis and is utilized in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. (3,5-dibromophenyl)(phenyl)methanol also finds use as an intermediate in the production of dyes, pigments, and specialty chemicals. Furthermore, it has potential applications in medicinal chemistry due to its interesting biological activities and pharmacological properties. However, its halogenated nature requires careful handling and adherence to safety precautions.

Uses

Used in Pharmaceutical Industry:
(3,5-dibromophenyl)(phenyl)methanol is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
(3,5-dibromophenyl)(phenyl)methanol is used as a starting material in the synthesis of agrochemicals, which are essential for the protection and enhancement of crop yields.
Used in Fine Chemicals Industry:
(3,5-dibromophenyl)(phenyl)methanol is utilized as an intermediate in the production of fine chemicals, which are important for various industrial applications.
Used in Dyes and Pigments Industry:
(3,5-dibromophenyl)(phenyl)methanol is used as an intermediate in the manufacture of dyes and pigments, which are crucial for coloring and enhancing the appearance of various products.
Used in Specialty Chemicals Industry:
(3,5-dibromophenyl)(phenyl)methanol is employed in the production of specialty chemicals, which have unique properties and applications in different industries.
Used in Medicinal Chemistry:
(3,5-dibromophenyl)(phenyl)methanol is used as a research tool in medicinal chemistry, where it exhibits interesting biological activities and pharmacological properties, potentially leading to the discovery of new therapeutic agents.

Upstream product

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

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 
• 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 
• 422550-94-5 1-[3-benzyl-5-(1,1-dioxoisothiazolidin-2-ylmethyl)-phenyl]-1-(8-hydroxy-[1,6]naphthyridin-7-yl)-methanone 

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