7371-69-9 Usage
Uses
Used in Materials Science:
Cyclobutane-1,1,3,3-tetracarboxylic acid serves as a building block in the synthesis of new polymers, owing to its ability to form multiple covalent bonds with other molecules. Its cyclic structure and carboxylic acid groups contribute to the creation of polymers with unique properties, such as enhanced stability and reactivity.
Used in Coordination Complexes:
In the field of coordination chemistry, cyclobutane-1,1,3,3-tetracarboxylic acid acts as a ligand, capable of forming stable complexes with various metal ions. Its chelating ability, facilitated by the four carboxylic acid groups, is utilized to create coordination complexes with potential applications in catalysis, sensing, and medicinal chemistry.
Used in Industrial Applications:
The strong acidity of cyclobutane-1,1,3,3-tetracarboxylic acid makes it suitable for use in various industrial processes that require acidic conditions. Its potential applications include the manufacturing of specialty chemicals, the development of acid catalysts for specific reactions, and the production of materials with tailored properties.
Used in Scientific Research:
Cyclobutane-1,1,3,3-tetracarboxylic acid is an intriguing compound for researchers due to its unique structure and functional groups. It is employed in scientific studies to explore its potential properties, such as its reactivity, stability, and interactions with other molecules. This research can lead to the discovery of new applications and the development of innovative materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 7371-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7371-69:
(6*7)+(5*3)+(4*7)+(3*1)+(2*6)+(1*9)=109
109 % 10 = 9
So 7371-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O8/c9-3(10)7(4(11)12)1-8(2-7,5(13)14)6(15)16/h1-2H2,(H,9,10)(H,11,12)(H,13,14)(H,15,16)
7371-69-9Relevant 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.
