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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, dimethoxy-, methyl ester

COC(=O)c1cccc(c1OC)OC Request for Quotation
Chemical Name: Benzoic acid, dimethoxy-, methyl ester
CAS Number: 2150-42-7
Product Number: AG003RLL(AGN-PC-0JLP4A)
Synonyms:
MDL No:
Molecular Formula: C10H12O4
Molecular Weight: 196.1999

Identification/Properties

Properties
MP:
48-52°C(lit.);
BP:
180-185 °C50 mm Hg(lit.)
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
196.202g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
196.074g/mol
Monoisotopic Mass:
196.074g/mol
Topological Polar Surface Area:
44.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
193
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


Methyl 2,3-dimethoxybenzoate is a versatile compound commonly used in chemical synthesis processes. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure and reactivity, this compound plays a crucial role in the development of new materials and products in the chemical industry. In organic synthesis, Methyl 2,3-dimethoxybenzoate can be utilized as a starting material for the preparation of more complex molecules through various reactions such as esterification, hydrogenation, and substitution reactions. Its presence in the synthesis process often leads to the formation of compounds with enhanced properties and functionalities, making it a valuable component in the production of a wide range of chemical products.