7403-22-7 Usage
Description
Octahydropentalene-1-carboxylic acid is a synthetic chemical compound characterized by a bicyclic ring system and a carboxylic acid functional group attached to one of the carbon atoms. It is a saturated and cyclic organic compound with eight carbon atoms arranged in a distinctive three-dimensional structure. octahydropentalene-1-carboxylic acid is not typically found in nature but can be created in the laboratory. Its unique structure and reactivity suggest potential applications in organic synthesis, medicinal chemistry, and material science, although further research is needed to explore its full potential.
Uses
Used in Organic Synthesis:
Octahydropentalene-1-carboxylic acid serves as a key intermediate in the synthesis of various organic compounds due to its unique bicyclic structure and carboxylic acid functionality, which can be utilized in a range of chemical reactions to form diverse products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, octahydropentalene-1-carboxylic acid may be employed as a building block for the development of new pharmaceuticals. Its specific structural features could be leveraged to design molecules with targeted biological activities, potentially leading to the creation of novel therapeutic agents.
Used in Material Science:
Octahydropentalene-1-carboxylic acid holds promise for use in material science, where its unique structure could contribute to the development of new materials with specialized properties. These materials could find applications in various industries, such as in the creation of advanced polymers, coatings, or other high-performance materials.
Further research and exploration of octahydropentalene-1-carboxylic acid's properties and applications are necessary to fully understand its potential utility in these and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 7403-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7403-22:
(6*7)+(5*4)+(4*0)+(3*3)+(2*2)+(1*2)=77
77 % 10 = 7
So 7403-22-7 is a valid CAS Registry Number.
7403-22-7Relevant articles and documents
Resolution and Absolute Configuration of Bicycloocta-2,6-diene-2-carboxylic Acid
Whitesell, James K.,Minton, Mark A.,Felman, Steven W.
, p. 2193 - 2195 (2007/10/02)
An efficient resolution of the title acid (1) by using (+)- and (-)-α-phenethylamine is described.The (+) acid was determined to be 1S by chemical correlation through (+)-cis-bicyclooctan-2-one (3) with (+)-cis-bicyclooct-7-en-endo-2-ol (4) where the absolute configuration is known to be 1R.The 1R configuration for (-)-3 was consistent with the negative Cotton effect observed for this ketone.
Acid catalyzed ring contractions in endo-2,8-trimethylene-cis-bicyclo[3.3.0]octylcations to methylperhydrotriquinacenes. One of the methyl extrusion processes in the tricycloundecane rearrangement
Fujikura, Yoshiaki,Takaishi, Naotake,Inamoto, Yoshiaki
, p. 4465 - 4477 (2014/12/10)
Sulfuric acid catalyzed ring contractions with extrusion of a methyl group were examined for alcohol and olefin derivatives (28-31) of endo-2,8-trimethylene-cis-bicyclo[3.3.0]octane (11), which was one of the two possible progenitors, among altogether 69 isomers, for methylperhydrotriquinacenes (6, 7 and 12), the only methyltricyctodecane intermediates found so far, in the tricycloundecane rearrangement. Only minor amounts (1.6-2.0%) of methylperhydrotriquinacenes were formed from these reactants 28-31, and the results support the earlier theoretical conclusion that the methyl extrusions were in general energetically quite unfavorable processes owing to the formation of primary carbinyl cations at the expense of more stable secondary bridge or tertiary bridgehead ones. Reaction pathways for these precursors 28-31 were discussed with reference to those of perhydrotriquinacene 2-carbinyl cations (33a's), which corresponded to some of the ring contraction product cations from 28-31.
