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(5-bromo-2-hydroxy-phenyl)-(4-methoxyphenyl)methanone, also known as BPMM, is an organic compound with the chemical formula C13H10BrO3. It is a ketone derivative that contains a bromine atom, a hydroxy group, and a methoxy group attached to a phenyl ring. BPMM has potential applications in the field of medicinal chemistry and pharmaceuticals due to its structural features and functional groups. It may be utilized in the synthesis of various biologically active compounds and pharmaceutical intermediates. (5-bromo-2-hydroxy-phenyl)-(4-methoxyphenyl)methanone's properties and potential uses make it of interest to researchers in drug discovery and development.

5445-83-0

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5445-83-0 Usage

Uses

Used in Medicinal Chemistry:
BPMM is used as a building block for the synthesis of biologically active compounds and pharmaceutical intermediates. Its unique structural features and functional groups make it a valuable component in the development of new drugs.
Used in Drug Discovery and Development:
BPMM is used as a research tool in drug discovery and development. Its properties and potential uses make it of interest to researchers working on the design and synthesis of new pharmaceutical agents.
Used in Pharmaceutical Industry:
BPMM is used as a key intermediate in the production of various pharmaceuticals. Its versatility and reactivity make it a valuable asset in the synthesis of a wide range of drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 5445-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5445-83:
(6*5)+(5*4)+(4*4)+(3*5)+(2*8)+(1*3)=100
100 % 10 = 0
So 5445-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H11BrO3/c1-18-11-5-2-9(3-6-11)14(17)12-8-10(15)4-7-13(12)16/h2-8,16H,1H3

5445-83-0Downstream Products

5445-83-0Relevant academic research and scientific papers

Rhodium-Catalyzed Directing-Group-Assisted Aldehydic C–H Arylations with Aryl Halides

Rao, Maddali L. N.,Ramakrishna, Boddu S.

, p. 5080 - 5093 (2017/09/20)

A rhodium-catalyzed general protocol for the directing-group-assisted arylation of aromatic aldehydic C–H bonds was developed. This method involves either hydroxy- or amino-group-directed aldehyde C–H arylation with various aryl halides. A broad synthetic scope for the preparation of 2-hydroxybenzophenones was established with electronically variant salicylaldehydes and aryl halides with chemo- and regioselective possibilities. The developed protocol was also applied in the synthesis of medicinally important 3-salicyloylpyridines in high yields.

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