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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)-

1,3-Cyclobutanediol, 2,2,4,4-tetramethyl-

OC1C(C)(C)C(C1(C)C)O Request for Quotation
Chemical Name: 1,3-Cyclobutanediol, 2,2,4,4-tetramethyl-
CAS Number: 3010-96-6
Product Number: AG0032WC(AGN-PC-0JLPZR)
Synonyms:
MDL No:
Molecular Formula: C8H16O2
Molecular Weight: 144.2114

Identification/Properties

Properties
MP:
126-129 °C(lit.)
BP:
220.3°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.5100 (estimate)
Computed Properties
Molecular Weight:
144.214g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
144.115g/mol
Monoisotopic Mass:
144.115g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
115
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2,4,4-Tetramethyl-1,3-cyclobutanediol is a crucial compound widely utilized in chemical synthesis processes. Its unique molecular structure and properties make it a highly versatile and valuable component in various applications.In chemical synthesis, this compound serves as an essential building block for the creation of specialized polymers, resins, and coatings. Its presence in formulations lends enhanced durability, chemical resistance, and stability to the final products. Additionally, 2,2,4,4-Tetramethyl-1,3-cyclobutanediol acts as a crosslinking agent, facilitating the formation of strong and resilient chemical bonds within complex molecular structures.Furthermore, this compound plays a significant role in the development of advanced materials such as adhesives, sealants, and composites. Its incorporation results in improved mechanical properties, adhesion strength, and thermal stability, making it an ideal choice for high-performance applications in various industries.Overall, the application of 2,2,4,4-Tetramethyl-1,3-cyclobutanediol in chemical synthesis is instrumental in the creation of innovative and durable products that meet the stringent requirements of modern industrial processes.