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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,2,3,4-Cyclobutanetetracarboxylic acid

OC(=O)C1C(C(=O)O)C(C1C(=O)O)C(=O)O Request for Quotation
Chemical Name: 1,2,3,4-Cyclobutanetetracarboxylic acid
CAS Number: 53159-92-5
Product Number: AG003D9P(AGN-PC-0JNZN5)
Synonyms:
MDL No:
Molecular Formula: C8H8O8
Molecular Weight: 232.14432

Identification/Properties

Properties
MP:
>238°C (dec.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
232.144g/mol
XLogP3:
-1.9
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
4
Exact Mass:
232.022g/mol
Monoisotopic Mass:
232.022g/mol
Topological Polar Surface Area:
149A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
292
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,2,3,4-Cyclobutanetetracarboxylic acid is a versatile compound commonly used in chemical synthesis for its unique structural properties. As a cyclic molecule containing four carboxylic acid groups, this acid serves as a crucial building block in the development of various organic compounds. One of the key applications of 1,2,3,4-Cyclobutanetetracarboxylic acid is in the synthesis of complex organic molecules, particularly in the formation of polycyclic systems and supramolecular structures. Its rigid and symmetrical structure allows for precise control over molecular arrangement and assembly, making it a valuable tool in the design of functional materials and pharmaceutical intermediates.In addition, the carboxylic acid groups present in this compound can participate in a range of chemical reactions, such as esterification, amidation, and metal coordination, enabling the modification and functionalization of the molecule for specific applications. These versatile reactivity properties make 1,2,3,4-Cyclobutanetetracarboxylic acid an essential component in the toolkit of organic chemists seeking to create novel molecules with tailored properties.