57544-12-4 Usage
Explanation
This is the chemical name of the compound, which is derived from its molecular structure and composition.
Explanation
This is an alternative identifier for the compound, which is used in research and scientific databases.
Explanation
Benzopyrans are a class of organic compounds that contain a benzene ring fused to a pyran ring. The compound in question belongs to this class.
Explanation
The compound has a complex molecular structure, which includes various functional groups and attachments to the benzene ring.
Explanation
The compound contains a nitro group (-NO2), a chlorophenyl group (a phenyl ring with a chlorine atom), and a methoxy group (-OCH3) attached to the benzene ring.
Explanation
The compound is a synthetic derivative of 2H-1-benzopyran, meaning it is a modified version of the parent compound with added functional groups.
Explanation
The main purpose of the compound is for research, as it has potential biological and pharmacological properties that are not yet well documented.
Explanation
The compound may have potential applications in the field of medicinal chemistry and drug development due to its biological and pharmacological properties.
Explanation
More research is required to fully understand the properties and potential uses of 2-(2-Chlorophenyl)-6-methoxy-3-nitro-2H-1-benzopyran.
Chemical class
Benzopyrans
Molecular structure
Complex
Functional groups
Nitro group, chlorophenyl group, methoxy group
Synthetic derivative
2H-1-benzopyran
Primary use
Research purposes
Potential applications
Medicinal chemistry and drug development
Further research needed
Yes
Check Digit Verification of cas no
The CAS Registry Mumber 57544-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,4 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57544-12:
(7*5)+(6*7)+(5*5)+(4*4)+(3*4)+(2*1)+(1*2)=134
134 % 10 = 4
So 57544-12-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H12ClNO4/c1-21-11-6-7-15-10(8-11)9-14(18(19)20)16(22-15)12-4-2-3-5-13(12)17/h2-9,16H,1H3
57544-12-4Relevant academic research and scientific papers
Augmentation of Enantioselectivity by Spatial Tuning of Aminocatalyst: Synthesis of 2-Alkyl/aryl-3-nitro-2 H-chromenes by Tandem Oxa-Michael-Henry Reaction
Bez, Ghanashyam,Mohanta, Rahul
, p. 4627 - 4636 (2020/05/01)
The asymmetric oxa-Michael addition of salicylaldehyde to conjugated nitroalkenes often suffers from poor reactivity and selectivity and a long reaction time. Because of the formation of an iminium ion with aminocatalyst, the nucleophilicity of the phenol
