CAS 736140-70-8

1H-Pyrrole, 1-[(2E)-3-(4-methoxyphenyl)-1-oxo-2-propenyl]-

Description:

1H-Pyrrole, 1-[(2E)-3-(4-methoxyphenyl)-1-oxo-2-propenyl]- is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing one nitrogen atom. This compound features a substituent that includes a 4-methoxyphenyl group and an α,β-unsaturated carbonyl moiety, contributing to its potential reactivity and biological activity. The presence of the methoxy group enhances its lipophilicity and may influence its interaction with biological targets. The compound's structure suggests it may participate in various chemical reactions, such as electrophilic substitutions or nucleophilic additions, due to the electron-rich nature of the pyrrole ring and the electrophilic carbonyl group. Additionally, compounds with similar structures have been studied for their pharmacological properties, including anti-inflammatory and anticancer activities. Its CAS number, 736140-70-8, allows for precise identification in chemical databases, facilitating research and application in medicinal chemistry and related fields.

Formula: C₁₄H₁₃NO₂

1-(4-Methoxycinnamoyl)pyrrole

CAS: 736140-70-8

Formula: C₁₄H₁₃NO₂

Purity: 98.5%

Molecular weight: 227.2585

Ref: IN-DA00FGQH

1-(4-Methoxycinnamoyl)pyrrole

CAS: 736140-70-8

1-(4-Methoxycinnamoyl)pyrrole is a natural product for research related to life sciences. The catalog number is TN2474 and the CAS number is 736140-70-8.

Formula: C₁₄H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 227.26

Ref: TM-TN2474

1-(4-Methoxycinnamoyl)pyrrole

CAS: 736140-70-8

Formula: C₁₄H₁₃NO₂

Purity: 95%~99%

Color and Shape: Powder

Molecular weight: 227.263

Ref: BP-SBP02896

1-(4-Methoxycinnamoyl)pyrrole

CAS: 736140-70-8

1-(4-Methoxycinnamoyl)pyrrole is a small organic compound, which is synthesized through the condensation of 4-methoxycinnamic acid and pyrrole. This compound is primarily derived from laboratory settings, specifically designed for research and potential therapeutic applications. The mode of action is believed to involve the inhibition of oxidative stress pathways and modulation of inflammatory responses, which might be mediated through its interaction with cellular signaling cascades.

Formula: C₁₄H₁₃NO₂

Purity: Min. 95%

Molecular weight: 227.26 g/mol

Ref: 3D-LEB14070