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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, 4-(methoxymethoxy)-

COCOc1ccc(cc1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 4-(methoxymethoxy)-
CAS Number: 25458-44-0
Product Number: AG003K8W(AGN-PC-005BF5)
Synonyms:
MDL No:
Molecular Formula: C9H10O4
Molecular Weight: 182.1733

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
182.175g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
182.058g/mol
Monoisotopic Mass:
182.058g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
161
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:
H302-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


4-(Methoxymethoxy)benzoic acid is a versatile compound used in various chemical processes, particularly in organic synthesis. Its unique structure and properties make it a valuable building block for creating complex organic molecules. In chemical synthesis, this compound can serve as a key intermediate for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its methoxy groups can undergo different reactions, such as esterification, amidation, and oxidation, enabling the synthesis of diverse compounds with specific functionalities. Additionally, the benzoic acid moiety in this compound provides a platform for further derivatization, allowing for the modification of its properties for specific applications. Overall, 4-(Methoxymethoxy)benzoic acid plays a crucial role in advancing the field of organic chemistry by enabling the efficient and precise construction of complex molecules for various industrial and academic purposes.