728885-46-9 Usage
Benzaldehyde derivative
A compound derived from benzaldehyde
2-[(2-Bromobenzyl)oxy]-3-methoxybenzaldehyde is a derivative of benzaldehyde, which means it is a compound obtained by modifying the structure of benzaldehyde.
Aldehyde group present
Functional group with a carbonyl group (C=O) at the end of a carbon chain
2-[(2-Bromobenzyl)oxy]-3-methoxybenzaldehyde contains an aldehyde group, which is a carbonyl group (C=O) bonded to a carbon atom at the end of a carbon chain, giving it specific chemical reactivity.
Methoxy group present
Functional group consisting of an oxygen atom connected to a methyl group (-OCH3)
The compound also contains a methoxy group, which is an oxygen atom connected to a methyl group (-OCH3), providing additional reactivity and properties.
Bromobenzyl ether functional group
A bromine-containing aromatic ether group
2-[(2-Bromobenzyl)oxy]-3-methoxybenzaldehyde has a bromobenzyl ether functional group, which is a bromine-containing aromatic ether group that contributes to its unique chemical structure and reactivity.
Potential applications in organic synthesis
Can be used as a building block or reactant in organic reactions
Potential applications in pharmaceutical research
Can be used as a precursor or intermediate in the synthesis of pharmaceutical compounds
Valuable for further study and exploration
Importance in the fields of chemistry and pharmacology
The properties and potential uses of 2-[(2-Bromobenzyl)oxy]-3-methoxybenzaldehyde make it a valuable compound for further study and exploration in the fields of chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 728885-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,8,8,8 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 728885-46:
(8*7)+(7*2)+(6*8)+(5*8)+(4*8)+(3*5)+(2*4)+(1*6)=219
219 % 10 = 9
So 728885-46-9 is a valid CAS Registry Number.
728885-46-9Relevant academic research and scientific papers
Synthesis and biological evaluation of dibenz[b,f][1,5]oxazocine derivatives for agonist activity at κ-opioid receptor
Mitra, Sudipta,Banerjee, Tuhin Suvro,Hota, Sandip K.,Bhattacharya, Debleena,Das, Sumantra,Chattopadhyay, Partha
scheme or table, p. 1713 - 1720 (2011/05/06)
A short and high yield synthetic route to dibenz[b,f][1,5]oxazocines has been developed using Pd catalyzed intramolecular cycloamination reaction. Receptor binding assay using [125I]-dynorphin demonstrated that one of the derivative, 5b showed
An efficient synthesis of novel dibenzo-fused nine-membered oxacycles using a sequential Baylis-Hillman reaction and radical cyclization
Majhi, Tirtha Pada,Neogi, Arpita,Ghosh, Soumen,Mukherjee, Alok Kumar,Helliwell, Madeleine,Chattopadhyay, Partha
, p. 94 - 100 (2008/09/20)
A short and high yield synthetic route to novel dibenz[b,g]oxonins, one of which has been characterized by X-ray crystallography, has been developed based on a sequential Baylis-Hillman reaction and radical cyclization. The regioselective radical cyclization followed a 9-endo-trig pathway. Georg Thieme Verlag Stuttgart.
