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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, 2,5-dimethoxy-

COc1ccc(c(c1)CO)OC Request for Quotation
Chemical Name: Benzenemethanol, 2,5-dimethoxy-
CAS Number: 33524-31-1
Product Number: AG003FYZ(AGN-PC-0077P2)
Synonyms:
MDL No:
Molecular Formula: C9H12O3
Molecular Weight: 168.1898

Identification/Properties

Properties
BP:
122°C at 1 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
168.192g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
168.079g/mol
Monoisotopic Mass:
168.079g/mol
Topological Polar Surface Area:
38.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
127
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

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


$Name$ is a versatile compound that finds extensive application in chemical synthesis, particularly in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. As a precursor molecule, (2,5-Dimethoxyphenyl)methanol serves as a key building block for the synthesis of more complex organic compounds. Its unique structure and reactivity make it a valuable starting material for the creation of diverse chemical entities with specific functionalities.In chemical synthesis, (2,5-Dimethoxyphenyl)methanol can be utilized as a key intermediate in the production of pharmaceutical drugs and fine chemicals. Its presence in the synthetic route enables the introduction of specific functional groups or modifications, leading to the desired end products. Through various chemical transformations such as oxidation, reduction, and substitution reactions, this compound can be tailored to yield a range of structurally diverse molecules with different properties and applications.Moreover, (2,5-Dimethoxyphenyl)methanol plays a crucial role in the development of new materials and compounds with targeted characteristics. By incorporating this compound into the synthesis of polymers, coatings, or other advanced materials, researchers and chemists can fine-tune the properties of the final products to meet specific requirements. Its ability to serve as a scaffold for molecular design makes it an indispensable tool in the field of organic synthesis and material science.Overall, the application of (2,5-Dimethoxyphenyl)methanol in chemical synthesis offers a wealth of opportunities for creating novel molecules, functional materials, and specialized chemicals essential for various industries and scientific research endeavors. Its versatile nature and reactivity make it a valuable asset in the hands of chemists and researchers seeking to innovate and advance the field of organic chemistry.