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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)-

2-Propenoic acid, 3-(4,5-dimethoxy-2-nitrophenyl)-

COc1cc(C=CC(=O)O)c(cc1OC)[N+](=O)[O-] Request for Quotation
Chemical Name: 2-Propenoic acid, 3-(4,5-dimethoxy-2-nitrophenyl)-
CAS Number: 20567-38-8
Product Number: AG002AA9(AGN-PC-0712SC)
Synonyms:
MDL No:
Molecular Formula: C11H11NO6
Molecular Weight: 253.2081

Identification/Properties

Properties
BP:
482.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
253.21g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
253.059g/mol
Monoisotopic Mass:
253.059g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
337
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


3-(4,5-Dimethoxy-2-nitrophenyl)acrylic acid is a versatile compound that finds widespread application in chemical synthesis due to its unique properties and reactivity. This compound serves as a key intermediate in the synthesis of various organic molecules and materials. Its functional groups, including the nitro and methoxy moieties, enable it to participate in a range of important chemical reactions.In organic synthesis, 3-(4,5-Dimethoxy-2-nitrophenyl)acrylic acid can be utilized as a building block for the construction of more complex structures. It can undergo reactions such as reduction, substitution, and condensation to introduce new functional groups and modify its chemical properties. The resulting derivatives of this compound can exhibit diverse biological activities or serve as precursors for the synthesis of pharmaceuticals, dyes, polymers, and other specialty chemicals.Additionally, the presence of the acrylic acid group in this compound offers opportunities for further functionalization through cross-coupling reactions or polymerization, leading to the creation of novel materials with tailored properties. Moreover, the structural features of 3-(4,5-Dimethoxy-2-nitrophenyl)acrylic acid make it a valuable intermediate in the development of advanced materials for applications in fields such as medicine, materials science, and agrochemicals.