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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)-

3,3-Dimethoxy-1-methyl-cyclobutanecarboxylic acid

COC1(OC)CC(C1)(C)C(=O)O Request for Quotation
Chemical Name: 3,3-Dimethoxy-1-methyl-cyclobutanecarboxylic acid
CAS Number: 1408075-28-4
Product Number: AG001CU0(AGN-PC-0WBS3J)
Synonyms:
MDL No: MFCD23106030
Molecular Formula: C8H14O4
Molecular Weight: 174.1944

Identification/Properties

Computed Properties
Molecular Weight:
174.196g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
174.089g/mol
Monoisotopic Mass:
174.089g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
187
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:
H302
Precautionary Statements:
P301+P312+P330
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,3-Dimethoxy-1-methylcyclobutanecarboxylic acid is a versatile chemical compound that finds widespread applications in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties and reactivity. In organic synthesis, 3,3-Dimethoxy-1-methylcyclobutanecarboxylic acid is commonly used as a precursor in the preparation of complex molecules that contain cyclobutane rings. Its cyclobutane motif can undergo diverse chemical transformations, such as ring-opening reactions, cycloadditions, and functional group manipulations, enabling the synthesis of structurally intricate compounds with diverse functionalities. Additionally, the presence of the dimethoxy and methyl groups in this compound imparts specific steric and electronic properties that can be exploited in designing and tailoring molecular structures for specific applications in the fields of medicinal chemistry, materials science, and organic synthesis.