1. Home
  2. Propanedioic acid, (2-methoxyphenoxy)-, dimethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Propanedioic acid, (2-methoxyphenoxy)-, dimethyl ester

COC(=O)C(C(=O)OC)Oc1ccccc1OC Request for Quotation
Chemical Name: Propanedioic acid, (2-methoxyphenoxy)-, dimethyl ester
CAS Number: 150726-89-9
Product Number: AG001MTQ(AGN-PC-00KAFN)
Synonyms:
MDL No: MFCD06797652
Molecular Formula: C12H14O6
Molecular Weight: 254.2360

Identification/Properties

Properties
BP:
320.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
254.238g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
7
Exact Mass:
254.079g/mol
Monoisotopic Mass:
254.079g/mol
Topological Polar Surface Area:
71.1A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
274
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Dimethyl 2-(2-methoxyphenoxy)malonate is a versatile compound commonly used in chemical synthesis as a key building block for a wide range of organic reactions. This compound serves as an important intermediate in the preparation of various functionalized molecules, such as pharmaceuticals, agrochemicals, and materials.In organic synthesis, Dimethyl 2-(2-methoxyphenoxy)malonate can undergo various transformations to introduce specific functional groups or structural motifs into a molecule. Its malonate moiety provides a reactive site for nucleophilic substitution reactions, enabling the introduction of new substituents. Additionally, the aromatic ether group offers opportunities for cross-coupling reactions and further functionalization.One common application of Dimethyl 2-(2-methoxyphenoxy)malonate is in the synthesis of biologically active compounds, where its presence as a building block allows chemists to efficiently construct complex molecules with desired pharmacological properties. By incorporating this compound into multi-step synthetic pathways, researchers can access diverse chemical space and develop novel drug candidates.Overall, Dimethyl 2-(2-methoxyphenoxy)malonate plays a crucial role in modern chemical synthesis by enabling the construction of structurally complex and functionally diverse molecules for various applications in science and industry.