CAS 3413-59-0
:Butoxyphenylacetamide; 98%
Description:
Butoxyphenylacetamide, with the CAS number 3413-59-0, is an organic compound characterized by its amide functional group and the presence of a butoxy group attached to a phenyl ring. This substance typically appears as a white to off-white solid and is known for its moderate solubility in organic solvents. It is often utilized in various chemical applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The compound exhibits properties such as stability under standard conditions, but it may be sensitive to moisture and light, necessitating proper storage conditions. Its molecular structure contributes to its potential biological activity, making it of interest in medicinal chemistry. Safety data sheets indicate that it should be handled with care, as it may pose health risks if ingested or inhaled, and appropriate personal protective equipment should be used during handling. Overall, butoxyphenylacetamide is a versatile compound with applications in research and industry, reflecting the importance of amides in organic synthesis.
Formula:C12H17NO2
InChI:InChI=1/C12H17NO2/c1-2-3-8-15-11-6-4-10(5-7-11)9-12(13)14/h4-7H,2-3,8-9H2,1H3,(H2,13,14)
InChI key:InChIKey=RSMPEQBSFXBQMJ-UHFFFAOYSA-N
SMILES:CCCCOc1ccc(cc1)CC(=N)O
Synonyms:- (4-Butoxyphenyl)acetamide
- 2-(4-Butoxyphenyl)Acetamide
- 4-Butoxybenzeneacetamide
- Acetamide, 2-(p-butoxyphenyl)-
- Benzeneacetamide, 4-butoxy-
- p-Butoxyphenylacetamide
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
BUFEXAMAC IMPURITY D CRS
CAS:<p>BUFEXAMAC IMPURITY D CRS</p>Formula:C12H17NO2Molecular weight:207.2689Bufexamac EP Impurity D
CAS:Controlled ProductFormula:C12H17NO2Color and Shape:NeatMolecular weight:207.27(4-Butoxyphenyl)acetamide
CAS:<p>4-Butoxyphenyl)acetamide is a synthetically produced chemoattractant that is used in vitro to study the migration of cells. It is soluble in non-polar solvents and can be expressed from many organisms, including bacteria and plants. 4-Butoxyphenyl)acetamide has been shown to induce cell movement by binding to the G protein coupled receptor that stimulates the release of calcium ions from intracellular stores. This molecule also has photophysical properties, which have been studied in rat liver microsomes and hydrochloric acid, hydroxamic acids, and spermatozoa. 4-Butoxyphenyl)acetamide can be absorbed from the intestine into plasma, where it binds to odorant receptors on sensory neurons in the nose. These receptors are also found in plant physiology, where they are responsible for detecting chemicals that attract pollinators such as bees or insects.</p>Formula:C12H17NO2Purity:Min. 90 Area-%Color and Shape:PowderMolecular weight:207.27 g/mol





