130252-84-5 Usage
Molecular structure
Consists of a naphthalene ring with various functional groups attached to it, including a carboxylic acid, methoxy, methyl, and an ester linkage.
Molecular weight
414.47 g/mol
Functional groups
Naphthalene ring, carboxylic acid, methoxy, methyl, and ester linkage.
Stereochemistry
The compound has two chiral centers, one at the ester linkage (1R) and another at the oxirane ring (2S).
Biological activity
The presence of various functional groups suggests potential biological activity or pharmaceutical relevance, but further research and analysis are necessary to confirm this.
Solubility
The compound's solubility properties are not well-known, but it is likely to be soluble in organic solvents due to its lipophilic nature.
Stability
The compound's stability is not well-known, but it may be sensitive to heat, light, or other environmental factors due to the presence of various functional groups.
Synthesis
The compound is likely synthesized through a series of chemical reactions involving the formation of the naphthalene ring, ester linkage, and attachment of functional groups.
Applications
The potential applications of 1-Naphthalenecarboxylic acid, 3-methoxy-5-methyl-,
(1R)-2-[(4-methoxyphenyl)methoxy]-1-[(2S)-2-methyloxiranyl]ethyl ester are not well-known, but its unique structure and functional groups may make it useful in pharmaceuticals, materials science, or other research areas. Further research and analysis are necessary to fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 130252-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,5 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130252-84:
(8*1)+(7*3)+(6*0)+(5*2)+(4*5)+(3*2)+(2*8)+(1*4)=85
85 % 10 = 5
So 130252-84-5 is a valid CAS Registry Number.
130252-84-5Relevant academic research and scientific papers
Synthetic studies of carzinophilin. Part 1: Synthesis of 2-methylidene-1-azabicyclo[3.1.0]hexane systems related to carzinophilin
Hashimoto, Masaru,Matsumoto, Miyoko,Terashima, Shiro
, p. 3019 - 3040 (2007/10/03)
Synthesis of the model compounds of carzinophilin carrying 2-methylidene-1-aza-bicyclo[3.1.0]hexane systems was achieved. Formation of malonylidenes or N-acyl-glycinylidenepyrrolidines was carried out by utilizing Eschenmoser's sulfide contraction or Herdeis's condensation between the 2-methylthio-Δ1-pyrrolone derivatives and ethyl nitroacetate, respectively. The 1-azabicyclo-[3.1.0]hexane systems were constructed by base-promoted aziridine formation.
Synthetic studies towards carzinophilin: Synthesis and ammonium hydroxide-induced rearrangement of the epoxi-acid fragment
England, Pamela,Chun, Keun Ho,Moran, Edmund J.,Armstrong, Robert W.
, p. 2669 - 2672 (2007/10/02)
An efficient synthesis of the epoxide-containing fragment 4 of carzinophilin has been completed. Intramolecular acyl transfer of a related epoxide afforded amide 16. Comparison by 1H NMR of 4 and 16 with authentic natural product provides further evidence for structural revision of carzinophilin.
