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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)-

Benzoic acid, 2-(methoxymethyl)-

COCc1ccccc1C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 2-(methoxymethyl)-
CAS Number: 88550-19-0
Product Number: AG004DOK(AGN-PC-0NI7WZ)
Synonyms:
MDL No:
Molecular Formula: C9H10O3
Molecular Weight: 166.1739

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
166.176g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
166.063g/mol
Monoisotopic Mass:
166.063g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
156
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Methoxymethyl)benzoic acid, also known as o-methoxymethylbenzoic acid, plays a crucial role in chemical synthesis as a versatile building block with various applications. This compound is commonly used as a starting material for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for selective functional group transformations, making it a valuable intermediate in organic synthesis.In chemical synthesis, 2-(Methoxymethyl)benzoic acid can undergo reactions such as esterification, amidation, and hydrogenation to introduce different functional groups at specific positions on the benzene ring. This flexibility enables chemists to tailor the compound's properties to suit specific applications.Additionally, the methoxy and methyl groups on the benzene ring provide opportunities for further derivatization, allowing for the synthesis of more complex molecules. By carefully controlling the reaction conditions, chemists can selectively modify the compound to achieve desired structural motifs and properties.Overall, 2-(Methoxymethyl)benzoic acid serves as a valuable building block in chemical synthesis, offering a platform for the creation of diverse molecules with potential applications in various industries.