CAS 6622-73-7

N-[4-(2-Propen-1-yloxy)phenyl]acetamide

Description:

N-[4-(2-Propen-1-yloxy)phenyl]acetamide, with the CAS number 6622-73-7, is an organic compound characterized by its amide functional group and a propenyl ether moiety. This compound features a phenyl ring substituted with a propenyloxy group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the acetamide group indicates that it may exhibit properties typical of amides, such as hydrogen bonding capabilities, which can influence its solubility and boiling point. Additionally, the propenyl group suggests that the compound may participate in polymerization reactions, making it of interest in materials science and polymer chemistry. Its structural characteristics may also impart specific biological activities, which could be explored in medicinal chemistry. Overall, N-[4-(2-Propen-1-yloxy)phenyl]acetamide is a versatile compound with potential applications in various fields, including pharmaceuticals and materials development.

Formula: C₁₁H₁₃NO₂

InChI: InChI=1/C11H13NO2/c1-3-8-14-11-6-4-10(5-7-11)12-9(2)13/h3-7H,1,8H2,2H3,(H,12,13)

InChI key: InChIKey=UVGQOPZEALYXKP-UHFFFAOYSA-N

SMILES: N(C(C)=O)C1=CC=C(OCC=C)C=C1

Synonyms:

• N-[4-(2-Propen-1-yloxy)phenyl]acetamide
• Acetamide, N-[4-(2-propen-1-yloxy)phenyl]-
• Acetamide, N-[4-(2-propenyloxy)phenyl]-
• 4-Acetamidophenyl allyl ether
• Acetanilide, 4′-(allyloxy)-
• 4-Allyloxyacetanilide,98%
• N-[4-(prop-2-en-1-yloxy)phenyl]acetamide
• N1-[4-(ALLYLOXY)PHENYL]ACETAMIDE
• 4-ALLYLOXYACETANILIDE
• 4’-allyloxy-acetanilid
• o-(2-Propenyloxy)acetanilide
• N-(4-prop-2-enoxyphenyl)acetamide

N1-[4-(allyloxy)phenyl]acetamide

CAS: 6622-73-7

N1-[4-(allyloxy)phenyl]acetamide

Purity: 95%

Molecular weight: 191.22642g/mol

Ref: 54-OR30189

N1-[4-(Allyloxy)phenyl]acetamide

CAS: 6622-73-7

N1-[4-(Allyloxy)phenyl]acetamide is a catalyst which is used to synthesize polyolefins, such as polyethylene and polypropylene. It has been shown to be an effective catalyst for the polymerization of ethylene. N1-[4-(Allyloxy)phenyl]acetamide has also been shown to have a high activity in the synthesis of polyolefins, with rates comparable to those of the most commonly used catalysts. The crystal structure of this compound was determined by X-ray diffraction analysis and found to contain two crystallographic asymmetric units. This complex can be immobilized on titanium or zirconium oxide supports and is soluble in dichloromethane. The molecular structure of N1-[4-(Allyloxy)phenyl]acetamide has been analyzed by X-ray crystallography and found to contain a planar acetamide group that is connected through a methylene bridge with an allyl

Formula: C₁₁H₁₃NO₂

Purity: Min. 95%

Molecular weight: 191.23 g/mol

Ref: 3D-GAA62273