22636-68-6

Basic information

• Product Name: allyl 4-(dimethylamino)benzoate
• Synonyms: allyl 4-(dimethylamino)benzoate
• CAS NO: 22636-68-6
• Molecular Weight: 205.257
• Mol File: 22636-68-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: allyl 4-(dimethylamino)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 4-(dimethylamino)benzoate(22636-68-6)
• EPA Substance Registry System: allyl 4-(dimethylamino)benzoate(22636-68-6)

Safety Data

• Hazardous Substances Data: 22636-68-6(Hazardous Substances Data)

Upstream product

• 4755-50-4 4-(dimethylamino)benzoyl chloride 
• 107-18-6 allyl alcohol 
• 619-84-1 p-N,N-dimethylaminobenzoic acid 
• 106-95-6 allyl bromide 

Downstream Products

• 619-84-1 p-N,N-dimethylaminobenzoic acid 

Relevant articles and documents

FUNCTIONAL SKIN COATING POLYMER

Film-forming polymers that contain covalently-attached or non-covalently bound light-filtering, e.g., UV-absorbing, compounds and their use as a skin-protectant coating, such as a sunscreen, are disclosed.

Enantioselective Three-Component Fluoroalkylarylation of Unactivated Olefins through Nickel-Catalyzed Cross-Electrophile Coupling

A nickel-catalyzed, enantioselective, three-component fluoroalkylarylation of unactivated alkenes with aryl halides and perfluoroalkyl iodides has been described. This cross-electrophile coupling protocol utilizes a chiral nickel/BiOx system as well as a pendant chelating group to facilitate the challenging three-component, asymmetric difunctionalization of unactivated alkenes, providing direct access to valuable chiral β-fluoroalkyl arylalkanes with high efficiency and excellent enantioselectivity. The mild conditions allow for a broad substrate scope as well as good functional group toleration.