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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)-

(1S)-1-(2,5-dimethoxyphenyl)ethanol

COc1ccc(c(c1)C(O)C)OC Request for Quotation
Chemical Name: (1S)-1-(2,5-dimethoxyphenyl)ethanol
CAS Number: 41038-40-8
Product Number: AG003CT1(AGN-PC-009YNK)
Synonyms:
MDL No: MFCD08442838
Molecular Formula: C10H14O3
Molecular Weight: 182.2164

Identification/Properties

Properties
MP:
98-99℃
BP:
309.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
182.219g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
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:
149
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#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(2,5-Dimethoxyphenyl)ethanol, also known as $name$, is a valuable compound used in chemical synthesis for its versatile applications. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique chemical structure and properties. In organic synthesis, 1-(2,5-Dimethoxyphenyl)ethanol can be utilized as a key intermediate for the synthesis of complex molecules such as heterocycles, natural products, and advanced materials. Its functional groups make it an important precursor in the development of new drug candidates, as well as in the production of fine chemicals with specific biological activities and physical properties. Additionally, 1-(2,5-Dimethoxyphenyl)ethanol offers opportunities for creating novel molecular scaffolds and designing innovative chemical entities with potential applications in the fields of medicinal chemistry, material science, and chemical biology. Explore the potential of 1-(2,5-Dimethoxyphenyl)ethanol in your chemical synthesis endeavors for the synthesis of diverse and complex molecules with targeted functionalities.