Phenol, 2-ethoxy-5-(1-propenyl)-


Chemical Name: Phenol, 2-ethoxy-5-(1-propenyl)-
CAS Number: 94-86-0
Product Number: AG003TZ7(AGN-PC-0148I8)
Synonyms:
MDL No:
Molecular Formula: C11H14O2
Molecular Weight: 178.2277

Identification/Properties


Properties
MP:
86-88 °C(lit.)
BP:
116°C/2mmHg(lit.)
Storage:
2-8℃;
Form:
Solid
Refractive Index:
1.5670 (estimate)
Computed Properties
Molecular Weight:
178.231g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
178.099g/mol
Monoisotopic Mass:
178.099g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
166
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H303-H315-H319
Precautionary Statements:
P264-P280-P302+P352-P312-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-Ethoxy-5-(prop-1-en-1-yl)phenol, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in various organic reactions, particularly in the field of medicinal chemistry and fragrance synthesis. Its aromatic structure and functional groups make it an ideal precursor for the synthesis of biologically active molecules and fine chemicals.In chemical synthesis, 2-Ethoxy-5-(prop-1-en-1-yl)phenol can be employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to undergo various functional group transformations, such as oxidation, alkylation, and acylation, allows for the generation of a diverse array of compounds with tailored properties. Additionally, the presence of the ethoxy and propenyl groups in its structure imparts specific characteristics to the final products, making it a valuable component in the creation of targeted chemical compounds.Furthermore, the strategic incorporation of 2-Ethoxy-5-(prop-1-en-1-yl)phenol in chemical reactions enables chemists to access new chemical entities with enhanced biological activities or improved physicochemical properties. Its reactivity and structural features contribute to the design and synthesis of potent drug candidates, natural product derivatives, and fragrances with unique olfactory profiles.Overall, 2-Ethoxy-5-(prop-1-en-1-yl)phenol plays a crucial role in advancing the field of chemical synthesis by serving as a versatile and reliable building block for the creation of novel compounds with diverse applications.