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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)-

Benzenemethanol, 4-(dimethoxymethyl)-

OCc1ccc(cc1)C(OC)OC Request for Quotation
Chemical Name: Benzenemethanol, 4-(dimethoxymethyl)-
CAS Number: 183057-64-9
Product Number: AG0024DF(AGN-PC-0KTLEU)
Synonyms:
MDL No:
Molecular Formula: C10H14O3
Molecular Weight: 182.2164

Identification/Properties

Properties
MP:
38-42°C
BP:
261℃
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
182.219g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
182.094g/mol
Monoisotopic Mass:
182.094g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
126
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4-(Dimethoxymethyl)phenyl)methanol, a versatile compound in chemical synthesis, is commonly utilized as a key building block in the production of various pharmaceuticals, agrochemicals, and organic materials. With its unique molecular structure, this compound plays a crucial role in the creation of complex organic compounds through its reactivity and compatibility with a wide range of other chemicals. Its functionality as a methylene-protected phenol group allows for selective transformations in organic reactions, facilitating the synthesis of intricate molecules with specific properties and functions. Additionally, the presence of methoxy groups enhances the compound's solubility and stability, making it a valuable reagent in the development of novel chemical entities. In summary, (4-(Dimethoxymethyl)phenyl)methanol serves as a valuable tool for chemists in the intricate realm of chemical synthesis, enabling the construction of diverse molecular architectures with precision and efficiency.