2398-16-5 Usage
Uses
Used in Organic Synthesis:
Cyclobutane-1,3-dicarboxylic acid serves as a valuable building block in organic synthesis, due to its unique cyclic structure and reactive carboxylic acid groups. It can be used to construct complex organic molecules and contribute to the development of novel chemical compounds.
Used in Polymer and Resin Production:
As a monomer, cyclobutane-1,3-dicarboxylic acid is utilized in the production of polymers and resins. Its cyclic structure and carboxylic acid groups facilitate the formation of polymer chains, enhancing the mechanical properties and thermal stability of the resulting materials.
Used as a Cross-linking Agent:
Cyclobutane-1,3-dicarboxylic acid functions as an effective cross-linking agent in the synthesis of organic materials. Its ability to form covalent bonds with other molecules allows for the creation of three-dimensional networks, improving the structural integrity and performance of the materials.
Used in Pharmaceutical Manufacturing:
Cyclobutane-1,3-dicarboxylic acid acts as a precursor in the manufacture of pharmaceuticals. Its chemical properties enable the synthesis of various drug molecules, contributing to the development of new therapeutic agents with potential applications in medicine.
Used in Agricultural Chemical Production:
Similarly, cyclobutane-1,3-dicarboxylic acid is employed as a precursor in the production of agricultural chemicals. Its incorporation into the chemical structures of agrochemicals can enhance their efficacy and selectivity, promoting more effective and sustainable agricultural practices.
Used in Biological and Pharmacological Research:
Cyclobutane-1,3-dicarboxylic acid has been studied for its potential biological and pharmacological activities. Its unique structure and functional groups may confer it with specific interactions with biological systems, offering opportunities for the discovery of new bioactive compounds and therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 2398-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2398-16:
(6*2)+(5*3)+(4*9)+(3*8)+(2*1)+(1*6)=95
95 % 10 = 5
So 2398-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O4/c7-5(8)3-1-4(2-3)6(9)10/h3-4H,1-2H2,(H,7,8)(H,9,10)
2398-16-5Relevant academic research and scientific papers
SYNTHESIS OF NEW CARBOCYCLIC ANALOGUES OF OXETANOCIN A AND OXETANOCIN G
Pecquet, Pascal,Huet, Francois,Legraverend, Michel,Bisagni, Emile
, p. 739 - 745 (2007/10/02)
The synthesis of cis-3-amino-1-cyclobutanemethanol has been performed in six steps (59.6percent yield) from cis-1,3-cyclobutanedicarboxylic anhydride.This allowed us to obtain two new carbocyclic analogues of oxetanocin A and oxetanocin G related to 7-deazaadenosine and 7-deazaguanosine.
On the Reduction of Benzvalene Ozonide to cis-1,3-Cyclobutanedimethanol with LiAlH4
Leininger, Hartmut,Lanzendoerfer, Franz,Christl, Manfred
, p. 669 - 680 (2007/10/02)
On treatment with LiAlH4 at -30 deg C the polymeric ozonide of benzvalene (1) gives bicyclobutane-endo,endo-2,4-dimethanol (7).At higher temperatures cis-1,3-cyclobutanedimethanol (4) is formed.The stereochemical course of this unusual C-C hydrogenolysis has been elucidated by means of deuterated substrates.For this purpose a complete analysis of 1H NMR spectra of the labeled cis-1,3-cyclobutanedicarboxylic anhydrides 9a-c had to be carried out.The dialcohol 7 and its bismethyl ether 16 add thiophenol across the central bond to form the cis products 18 and 19, respectively.Acids or Ag+ ions isomerize 7 via cleavage of a lateral bond into the ethers 21.
Ueber die Thermolyse von cis- und trans-1,3-Divinylcyclobutan
Schwarz, Wolfgang,Trautmann, Walter,Musso, Hans
, p. 990 - 993 (2007/10/02)
At 300 deg C cis-1,3-divinylcyclobutane (4) gives butadiene (5) and 4-vinyl-1-cyclohexene (6) as well as trans-1,3-divinylcyclobutane (2) in small quantity. 2 has been synthesized in an independent way and yields the same products as 4.The diradical 3 is
