7507-86-0 Usage
Description
2-Bromo-5-methoxybenzaldehyde is an organic compound that features a bromine atom at the 2nd position and a methoxy group at the 5th position on a benzene ring, with an aldehyde functional group attached to the 1st position. This chemical structure endows it with unique properties and reactivity, making it a versatile intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
2-Bromo-5-methoxybenzaldehyde is used as a key intermediate in the synthesis of Benzimidazole Quinolines, which are important for the development of new pharmaceutical compounds. These Benzimidazole Quinolines possess potential therapeutic properties and can be utilized in the treatment of various diseases.
Used in Chemical Synthesis:
2-Bromo-5-methoxybenzaldehyde is used as a building block in the preparation of Cyclopentenes, which are five-membered ring compounds with one carbon-carbon double bond. These Cyclopentenes are valuable in the synthesis of various organic compounds and can be found in natural products, pharmaceuticals, and materials science.
Used in Organic Chemistry Research:
2-Bromo-5-methoxybenzaldehyde is used as a precursor in the synthesis of Polycycles and Benzocarbocycles/N-Heterocycle derivatives. These complex ring systems are of significant interest in organic chemistry due to their potential applications in drug discovery, agrochemicals, and functional materials. The unique structural features of 2-Bromo-5-methoxybenzaldehyde allow for the efficient construction of these intricate molecular frameworks.
Check Digit Verification of cas no
The CAS Registry Mumber 7507-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7507-86:
(6*7)+(5*5)+(4*0)+(3*7)+(2*8)+(1*6)=110
110 % 10 = 0
So 7507-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO2/c1-11-7-3-2-6(5-10)8(9)4-7/h2-5H,1H3
7507-86-0Relevant articles and documents
Elaboration of the isochromane system of stephaoxocanes employing an Oxa-Pictet Spengler type cyclization
Kaufman, Teodoro S.,Bernardi, Carmem R.,Cipulli, Marcos,Silveira, Claudio C.
, p. 493 - 494 (2000)
An approach to the synthesis of the isochromane moiety embodying the AC-ring system of the stephaoxocanes, by the use of an Oxa-Pictet Spengler type cyclization strategy, is reported.
COMPOUNDS AND COMPOSITIONS FOR USE IN TREATING SKIN DISORDERS
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Paragraph 0592; 0620-0622, (2021/08/06)
Provided herein is a compound of formula (XXXII) or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer thereof or a physiologically functional derivative thereof, wherein R1, R2, R3, G, A, E, n, p, and q are defined herein. Also provided herein are compositions comprising a compound of formula (XXXII), and methods of using a compound of formula (XXXII), e.g., in the treatment or prevention of skin disorders.
A novel donor-π-acceptor anthracene monomer: Towards faster and milder reversible dimerization
Van Damme, Jonas,van den Berg, Otto,Brancart, Joost,Van Assche, Guy,Du Prez, Filip
, p. 912 - 920 (2019/01/16)
A novel functional 2,6-substituted donor-acceptor anthracene derivative, bearing a long alkyl spacer and a polymerizable end-group, is synthesized from readily available compounds. This monomer possesses conjugated electron donor and acceptor moieties to achieve UV absorption and anthracene dimerization at higher wavelengths and under milder conditions, than anthracene and other reported anthracene derivatives. The compound was shown to absorb at higher wavelengths and dimerize much faster compared to most 9-substituted anthracenes. The fast photochemical and relatively slow thermal scission of the dimers were studied and related to the chemical structure, i.e. the 2,6-substitution.
