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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)-

methyl 2-(7-hydroxy-1-benzofuran-3-yl)acetate

COC(=O)Cc1cc2c(o1)c(O)ccc2 Request for Quotation
Chemical Name: methyl 2-(7-hydroxy-1-benzofuran-3-yl)acetate
CAS Number: 181052-63-1
Product Number: AG0022MP(AGN-PC-00F3W1)
Synonyms:
MDL No: MFCD09991503
Molecular Formula: C11H10O4
Molecular Weight: 206.1947

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
206.197g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
206.058g/mol
Monoisotopic Mass:
206.058g/mol
Topological Polar Surface Area:
59.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
241
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-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-(7-hydroxybenzofuran-3-yl)acetate is a versatile compound used in chemical synthesis for various applications. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows for diverse functionalization and modification, making it a valuable building block for creating complex molecules. In addition, its reactivity and stability profile make it suitable for use in different types of transformations, such as esterification, acylation, and nucleophilic substitution reactions. The presence of the hydroxybenzofuran moiety further enhances the compound's potential for biological activity, potentially leading to the development of new compounds with therapeutic properties. Overall, Methyl 2-(7-hydroxybenzofuran-3-yl)acetate plays a crucial role in advancing synthetic chemistry and drug discovery efforts.