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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)-

Naphthalene, 2,3-dimethoxy-

COc1cc2ccccc2cc1OC Request for Quotation
Chemical Name: Naphthalene, 2,3-dimethoxy-
CAS Number: 10103-06-7
Product Number: AG0003LN(AGN-PC-0JTNKM)
Synonyms:
MDL No:
Molecular Formula: C12H12O2
Molecular Weight: 188.2225

Identification/Properties

Properties
MP:
116.5-120.5 °C(lit.);
BP:
295.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dimethoxynaphthalene is a versatile chemical compound frequently utilized in organic synthesis for its unique properties and reactivity. As a substituted naphthalene derivative, this compound serves as a valuable building block for the creation of various other organic compounds, particularly in the field of medicinal chemistry and material science.In chemical synthesis, 2,3-Dimethoxynaphthalene can act as an important intermediate in the preparation of complex molecules due to its ability to undergo various functional group transformations. Its methoxy groups can be selectively modified, allowing for the introduction of different substituents to tailor the molecular structure for specific applications.Furthermore, 2,3-Dimethoxynaphthalene can participate in a range of reactions such as electrophilic aromatic substitution, nucleophilic aromatic substitution, and transition metal-catalyzed cross-coupling reactions. These chemical transformations enable the synthesis of biologically active compounds, organic dyes, liquid crystals, and other functional materials.Overall, the use of 2,3-Dimethoxynaphthalene in chemical synthesis offers chemists a strategic tool to construct complex organic molecules with desired properties, making it a valuable component in the toolbox of synthetic chemists.