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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)-

2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-carboxylic acid

OC(=O)c1cccc2c1OC(C2)(C)C Request for Quotation
Chemical Name: 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-carboxylic acid
CAS Number: 42327-95-7
Product Number: AG00C8NZ(AGN-PC-0WAKEI)
Synonyms:
MDL No:
Molecular Formula: C11H12O3
Molecular Weight: 192.2112

Identification/Properties

Computed Properties
Molecular Weight:
192.214g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
192.079g/mol
Monoisotopic Mass:
192.079g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
247
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,2-Dimethyl-2,3-dihydrobenzofuran-7-carboxylic acid, commonly known as $name$, serves as a versatile building block in chemical synthesis due to its unique structural properties. This compound finds widespread application in organic chemistry as a crucial intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its specific molecular structure allows it to participate in a range of transformations, enabling the construction of complex molecular architectures with high efficiency and precision. In particular, $name$ serves as a key starting material for the synthesis of biologically active molecules, making it an essential component in the development of new drugs and innovative chemical entities. Additionally, its reactivity and compatibility with a variety of functional groups make it a valuable tool for the construction of diverse chemical structures, highlighting its significance in modern synthetic chemistry practices.