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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)-

1,2-Propanediol, 3-(4-methoxyphenoxy)-

OCC(COc1ccc(cc1)OC)O Request for Quotation
Chemical Name: 1,2-Propanediol, 3-(4-methoxyphenoxy)-
CAS Number: 17131-52-1
Product Number: AG0077QX(AGN-PC-0JKJZJ)
Synonyms:
MDL No:
Molecular Formula: C10H14O4
Molecular Weight: 198.2158

Identification/Properties

Computed Properties
Molecular Weight:
198.218g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
198.089g/mol
Monoisotopic Mass:
198.089g/mol
Topological Polar Surface Area:
58.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
143
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


3-(4-Methoxyphenoxy)propane-1,2-diol is a versatile compound commonly utilized in chemical synthesis as a building block for the creation of various organic molecules. Its unique structure, featuring both a methoxyphenyl and a diol moiety, lends itself well to a variety of transformations in organic reactions.This compound can serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. In particular, its phenolic group can undergo functionalization reactions to introduce additional substituents, allowing for the creation of a diverse array of derivatives with different properties and applications.Furthermore, 3-(4-Methoxyphenoxy)propane-1,2-diol can participate in ether formation reactions, leading to the synthesis of complex organic compounds with ether functionalities. This ability to form ether linkages is crucial in the construction of more intricate molecules, making this compound valuable in the development of advanced materials and specialty chemicals.Overall, the strategic placement of functional groups in 3-(4-Methoxyphenoxy)propane-1,2-diol makes it a valuable tool in chemical synthesis, offering chemists a versatile platform for the construction of diverse organic compounds with a range of potential applications.