130520-33-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 20 carbon (C), 20 hydrogen (H), 2 oxygen (O), and 1 sulfur (S) atoms.
Explanation
The compound consists of a cyclohexene ring (a six-membered ring with one double bond), a propanal group (a three-carbon chain with an aldehyde group at the end), a ketone group (a carbonyl group bonded to two other carbons), and a naphthalenylthio group (a naphthalene with a sulfur atom attached).
3. Synthetic organic compound
Explanation
1-Cyclohexene-1-propanal, 2-(2-naphthalenylthio)-3-oxo- is artificially synthesized, meaning it is not found naturally in the environment. It is classified as an organic compound because it contains carbon and hydrogen atoms.
Explanation
Due to its unique structure and properties, 1-Cyclohexene-1-propanal, 2-(2-naphthalenylthio)-3-oxomay have various applications in the fields of chemistry and pharmaceuticals. These applications can include the development of new drugs, chemical reactions, or as intermediates in the synthesis of other compounds.
5. Context-dependent uses and effects
Explanation
The specific uses and effects of 1-Cyclohexene-1-propanal, 2-(2-naphthalenylthio)-3-oxo- may vary depending on the context in which it is used and the intended application. For example, it may have different properties and uses in a chemical reaction compared to its role in a pharmaceutical compound.
Structure
Cyclohexene ring, propanal group, ketone, and naphthalenylthio substituent
Potential applications
Chemistry and pharmaceuticals
Check Digit Verification of cas no
The CAS Registry Mumber 130520-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,2 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130520-33:
(8*1)+(7*3)+(6*0)+(5*5)+(4*2)+(3*0)+(2*3)+(1*3)=71
71 % 10 = 1
So 130520-33-1 is a valid CAS Registry Number.
130520-33-1Relevant academic research and scientific papers
Tandem Photocyclization-Intramolecular Addition Reactions of Aryl Vinyl Sulfides. Observation of a Novel Cycloaddition-Allylic Sulfide Rearrangement
Dittami, James P.,Nie, Xiao Yi,Nie, Hong,Ramanathan, H.,Buntel, C.,et al.
, p. 1151 - 1158 (2007/10/02)
Photocyclization of aryl vinyl sulfides reportedly proceeds via thiocarbonyl ylide intermediates.The photochemical behavior of several aryl vinyl sulfides, which incorporate a pendant alkene side chain, was explored.In general, naphthyl and phenyl vinyl thioethers provided products which are consistent with photocyclization to a thiocarbonyl ylide intermediate followed by either intramolecular hydrogen shift or subsequent intramolecular ylide-alkene addition.Product distribution is influenced by solvent and and temperature effects.Novel secondary photoprocesses were also observed during some reactions.Thus, irradiation of naphthyl vinyl sulfide 20 gave dihydrothiophene 22 which underwent subsequent intramolecular cycloaddition to provide 24.Upon prolonged irradiation 24 undergoes a novel allylic sulfide rearrangement to provide 25.
PHOTOINITIATED INTRAMOLECULAR YLIDE-ALKENE CYCLOADDITION REACTIONS
Dittami, James P.,Nie, Xiao-Yi,Buntel, Christopher J.,Rigatti, Steven
, p. 3821 - 3824 (2007/10/02)
The intramolecular olefin addition reactions of phototransient species were investigated.Photolysis of aryl vinyl sulfides which incorporate the ethyl butenoate functional group provide ene-like products and/or (3+2) adducts.Product formation is governed
