67461-24-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 10 hydrogen (H) atoms, and 3 oxygen (O) atoms.
Explanation
The compound belongs to a specific class of chemical compounds known as benzodioxepins, which are characterized by a benzene ring fused to a dioxepin ring.
Explanation
The systematic name is a unique identifier for the compound based on the IUPAC nomenclature rules, which provide a standardized way of naming chemical compounds.
Explanation
The compound's structure consists of a benzene ring (six carbon atoms) fused to a dioxepin ring (seven carbon atoms), and a methoxy group (-OCH3) is attached to the third carbon atom of the benzene ring.
Explanation
The compound is commonly used as a precursor or intermediate in the production of various drugs and biologically active molecules, making it valuable in the fields of organic synthesis and pharmaceutical research.
Explanation
The compound's potential pharmacological properties and biological activities make it a significant target for medicinal chemistry and drug discovery, as it may lead to the development of new therapeutic agents.
Explanation
Due to its unique molecular structure and potential pharmacological properties, 1,5-dihydro-3-methoxy-2,4-benzodioxepin is considered an important target for research in medicinal chemistry and drug discovery, with the aim of developing new drugs and therapies.
Class
Benzodioxepin compounds
Molecular Structure
Six-membered benzene ring fused to a seven-membered dioxepin ring, with a methoxy group attached to the third carbon atom
Application
Organic synthesis and pharmaceutical research
Pharmacological Properties
Potential biological activities
Significance
Target for medicinal chemistry and drug discovery
Check Digit Verification of cas no
The CAS Registry Mumber 67461-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67461-24:
(7*6)+(6*7)+(5*4)+(4*6)+(3*1)+(2*2)+(1*4)=139
139 % 10 = 9
So 67461-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-11-10-12-6-8-4-2-3-5-9(8)7-13-10/h2-5,10H,6-7H2,1H3
67461-24-9Relevant articles and documents
Blanchette,A.,Sauriol-Lord,F.
, p. 4055 (1978)
Cyclic acetals as precursors of substituted isochromans and naphthoxepines
Garcia, Daniel,Foubelo, Francisco,Yus, Miguel
, p. 507 - 519 (2008/09/18)
The reaction of 6,8-dioxabenzocycloheptenes 3 or 8,10-dioxacycloocta[de]naphthalenes 5 [easily prepared from the dibenzylic diols 1 and 4, respectively, and a carbonyl compound] with an excess of lithium and a catalytic amount of DTBB (2.5 mol %) in THF a
Synthesis of carbohydrates via tandem use of the osmium-catalyzed asymmetric dihydroxylation and enzyme-catalyzed aldol addition reactions
Henderson, Ian,Sharpless, K. Barry,Wong, Chi-Huey
, p. 558 - 561 (2007/10/02)
A new strategy is described for the asymmetric synthesis of carbohydrate derivatives via the tandem use of the osmium-catalyzed asymmetric dihydroxylation (AD) and aldolase-catalyzed aldol addition reactions. Both D- and L-forms of fructose, 6-deoxy-galacto-2-heptulose, and 6-phenyl-galacto-2-hexulose were synthesized to illustrate this methodology.
