85553-51-1 Usage
Description
2-(3-Bromophenyl)furan is a chemical compound characterized by the molecular formula C10H6BrO. It is a derivative of furan, which is a heterocyclic compound with a five-membered ring consisting of four carbon atoms and one oxygen atom. The distinctive feature of 2-(3-Bromophenyl)furan is the presence of a bromine atom and a phenyl group attached to the furan ring. This structural composition endows it with potential utility in various fields such as organic synthesis, medicinal chemistry, pharmaceutical development, agrochemicals, and materials science. 2-(3-BROMOPHENYL)FURAN serves as a valuable building block for synthesizing more complex molecules and may possess biological activities that are beneficial in drug discovery and development.
Uses
Used in Organic Synthesis:
2-(3-Bromophenyl)furan is utilized as a key intermediate in organic synthesis for the creation of a variety of complex organic molecules. Its unique structure allows for further functionalization and modification, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(3-Bromophenyl)furan is employed as a structural element in the design and synthesis of new drug candidates. Its presence in a molecule can influence pharmacokinetic and pharmacodynamic properties, potentially leading to the development of more effective and safer medications.
Used in Pharmaceutical Development:
2-(3-Bromophenyl)furan is used as a building block in the development of pharmaceuticals, where its specific structural features may contribute to the biological activity of the resulting compounds. It may be incorporated into drug molecules to enhance their therapeutic effects or to improve their delivery to target sites within the body.
Used in Agrochemicals:
In agrochemical applications, 2-(3-Bromophenyl)furan may be used as a component in the synthesis of new pesticides, herbicides, or other crop protection agents. Its chemical properties could be harnessed to create molecules with improved efficacy, selectivity, and environmental compatibility.
Used in Materials Science:
2-(3-Bromophenyl)furan also finds use in materials science, where it may be incorporated into the development of new materials with specific properties. Its unique structure could contribute to the creation of materials with tailored characteristics for use in various industries, such as electronics, coatings, or advanced composites.
Check Digit Verification of cas no
The CAS Registry Mumber 85553-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,5 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85553-51:
(7*8)+(6*5)+(5*5)+(4*5)+(3*3)+(2*5)+(1*1)=151
151 % 10 = 1
So 85553-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrO/c11-9-4-1-3-8(7-9)10-5-2-6-12-10/h1-7H
85553-51-1Relevant articles and documents
Black phosphorus as a metal-free, visible-light-active heterogeneous photoredox catalyst for the direct C-H arylation of heteroarenes
Kalay, Erbay,Kü?ükke?eci, Hüseyin,Kilic, Haydar,Metin, ?nder
supporting information, p. 5901 - 5904 (2020/06/04)
Black phosphorus (BP) is for the first time employed as a metal-free, heterogeneous photoredox catalyst for the direct C-H arylation of heteroarenes with aryl diazonium salts. The arylated heteroarenes are obtained in moderate to good yields under visible-light illumination, and the protocol is shown to be applicable for the scale-up synthesis.
Porphyrin-Catalyzed Photochemical C–H Arylation of Heteroarenes
Rybicka-Jasińska, Katarzyna,K?nig, Burkhard,Gryko, Dorota
supporting information, p. 2104 - 2107 (2017/04/24)
Organic dyes are a promising class of photoredox catalysts and offer a meaningful alternative to broadly applied Ru and Ir complexes. We found that porphyrins with tuned physicochemical properties, by tailoring various substituents at the periphery of the
Gold(III) porphyrin-catalyzed cycloisomerization of allenones
Zhou, Cong-Ying,Chan, Philip Wai Hong,Che, Chi-Ming
, p. 325 - 328 (2007/10/03)
Gold(III) porphyrin-catalyzed cycloisomerization of allenones gave the corresponding furans in good to excellent yields (up to 98%) and with quantitative substrate conversions. By recovering the Au(III) catalyst, a recyclable catalytic system is developed with over 8300 product turnovers attained for the cycloisomerization of 1-phenyl-buta-2,3-dien-1-one. The versatility of the gold(III) porphyrin catalyst was exemplified by its application to the hydroamination and hydration of phenylacetylene in 73% and 87% yield, respectively.
