5336-61-8

Basic information

• Product Name: (2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide
• Synonyms: 2-propenamide, 2-cyano-3-(1-naphthalenyl)-, (2E)-
• CAS NO: 5336-61-8
• Molecular Formula: C₁₄H₁₀N₂O
• Molecular Weight: 222.242
• Mol File: 5336-61-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 505.1°C at 760 mmHg
• Flash Point: 259.3°C
• Density: 1.269g/cm³
• Vapor Pressure: 2.5E-10mmHg at 25°C
• Refractive Index: 1.703
• CAS DataBase Reference: (2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide(5336-61-8)
• EPA Substance Registry System: (2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide(5336-61-8)

Safety Data

• Hazardous Substances Data: 5336-61-8(Hazardous Substances Data)

Usage

General Description

The chemical "(2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide" is an organic compound with the molecular formula C17H11NO. It is classified as an enamide, containing a naphthalene ring and a cyano group. (2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide is commonly used in organic synthesis and pharmaceutical research due to its potential pharmacological properties. It is also used as a building block in the production of various pharmaceuticals and agrochemicals. The chemical structure of "(2E)-2-cyano-3-(naphthalen-1-yl)prop-2-enamide" provides a platform for the development of new drugs and compounds with potential medicinal and industrial applications.

Upstream product

• 25309-43-7 2-ethyl-hexanoic acid isopropenyl ester 
• 570-08-1 diethyl acetylmalonate 

Relevant articles and documents

Ethyl-branched aldehydes, ketones, and diketones from caimans (Caiman and Paleosuchus; Crocodylia, Reptilia)

Secretions from the paracloacal glands of alligators (Alligator spp.) and caimans (Caiman spp., Melanosuchus niger, and Paleosuchus spp.) were examined by GC-MS. The secretions of the common caiman (C. crocodilus), the broad-snouted caiman (C. latirostris), the yacare caiman (C. yacare), the dwarf caiman (P. palpebrosus), and the smooth-fronted caiman (P. trigonatus) yielded a new family of 43 aliphatic carbonyl compounds that includes aldehydes, ketones, and β-diketones with an ethyl branch adjacent to the carbonyl group. The identification of these glandular components and the syntheses and stereochemical investigations of selected compounds are described.