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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)-

Phenol, 2,4-dimethoxy-

COc1ccc(c(c1)OC)O Request for Quotation
Chemical Name: Phenol, 2,4-dimethoxy-
CAS Number: 13330-65-9
Product Number: AG0014KX(AGN-PC-0JTG8M)
Synonyms:
MDL No:
Molecular Formula: C8H10O3
Molecular Weight: 154.1632

Identification/Properties

Computed Properties
Molecular Weight:
154.165g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
154.063g/mol
Monoisotopic Mass:
154.063g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
116
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

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Chemical Structure


2,4-Dimethoxyphenol, also known as hydroquinone dimethyl ether, finds extensive application in chemical synthesis due to its versatile reactivity and unique properties. This compound serves as a valuable building block in the production of various pharmaceuticals, fragrances, and specialty chemicals. In chemical synthesis, 2,4-Dimethoxyphenol acts as a precursor for the synthesis of more complex molecules, serving as a key intermediate in organic reactions.One notable application of 2,4-Dimethoxyphenol is its use in the synthesis of dyes and pigments. By undergoing controlled chemical transformations, this compound can be converted into chromophores that impart vibrant colors to textiles, plastics, and cosmetics. Additionally, 2,4-Dimethoxyphenol is utilized in the production of antioxidants and polymer additives, enhancing the stability and durability of various materials.In the realm of medicinal chemistry, 2,4-Dimethoxyphenol plays a crucial role as a starting material for the synthesis of bioactive molecules. By incorporating this compound into the molecular structure of pharmaceutical agents, researchers can modulate their biological activity and optimize their therapeutic effects. Furthermore, 2,4-Dimethoxyphenol serves as a valuable reagent in the synthesis of natural products and biologically active compounds, contributing to the development of novel drugs and research chemicals.Overall, the application of 2,4-Dimethoxyphenol in chemical synthesis encompasses a wide range of industries and research fields, highlighting its significance as a versatile building block with diverse functionalities.