201610-44-8

Basic information

• Product Name: 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]- (9CI)
• Synonyms: 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]- (9CI);2-PropenaMide, N-[2-(3,4-dihydroxyphenyl)ethyl]-;N-[2-(3,4-Dihydroxyphenyl)ethyl]-2-propenamide
• CAS NO: 201610-44-8
• Molecular Formula: C₁₁H₁₃NO₃
• Molecular Weight: 207.22582
• Product Categories: ALCOHOL
• Mol File: 201610-44-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 496℃
• Flash Point: 254℃
• Appearance: /
• Density: 1.221
• CAS DataBase Reference: 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]- (9CI)(201610-44-8)
• EPA Substance Registry System: 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl]- (9CI)(201610-44-8)

Safety Data

• Hazardous Substances Data: 201610-44-8(Hazardous Substances Data)

Usage

Description

2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl](9CI) is a chemical compound that belongs to the class of amides. It is characterized by the presence of a propenamide group and an aromatic ring with hydroxyl groups, which are important structural features for its activity. 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl](9CI) may also possess antioxidant properties due to the presence of hydroxyl groups.

Uses

Used in Pharmaceutical Industry:
2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl](9CI) is used as a potential therapeutic agent for its potential pharmacological properties. Its structural features, including the propenamide group and aromatic ring with hydroxyl groups, contribute to its activity and potential applications in the development of new drugs.
Used in Antioxidant Applications:
Due to the presence of hydroxyl groups, 2-Propenamide, N-[2-(3,4-dihydroxyphenyl)ethyl](9CI) may also be used as an antioxidant in various applications. Further research is needed to fully understand its antioxidant potential and possible uses in different industries.

Upstream product

• 62-31-7 dopamine hydrochloride 
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Downstream Products

• 1413516-28-5 N-(2-[3,4-ditriethylsilyloxyphenyl]ethyl)acrylamide 

Relevant articles and documents

Robust magnetic double-network hydrogels with self-healing, MR imaging, cytocompatibility and 3D printability

Herein, we have fabricated a novel robust self-healing magnetic double-network hydrogel by multiple interactions between bondable magnetic Fe3O4 and chitosan-polyolefin matrix, and the hydrogel also exhibits an excellent magnetogenic effect and MR imageability. The practical potential of the magnetic double-network hydrogel is further revealed by its 3D-printing performance.

Carbohydrate-Responsive Surface Adhesion Based on the Dynamic Covalent Chemistry of Phenylboronic Acid- and Catechol-Containing Polymer Brushes

A glue, based on dynamic covalent chemistry, with a strong adhesion (2.38 kg cm?2), water resistance and carbohydrate responsive reversibility is presented. Using surface initiated atom transfer radical polymerization (SI-ATRP), glass and silicon surfaces were coated with copolymers functionalized with phenylboronic acids and catechols. In combination with microcontact printing (μCP) these polymer brushes give access to a carbohydrate responsive “supramolecular Velcro”.

Cooperativity of Catechols and Amines in High-Performance Dry/Wet Adhesives

The outstanding adhesive performance of mussel byssal threads has inspired materials scientists over the past few decades. Exploiting the amino-catechol synergy, polymeric pressure-sensitive adhesives (PSAs) have now been synthesized by copolymerizing tra