64723-73-5

Basic information

• Product Name: [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE
• Synonyms: [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE
• CAS NO: 64723-73-5
• Molecular Formula: C₁₂H₁₅N
• Molecular Weight: 173.2542
• Mol File: 64723-73-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 240.1 °C at 760 mmHg
• Flash Point: 90.6 °C
• Appearance: /
• Density: 0.86 g/cm³
• Vapor Pressure: 0.0599mmHg at 25°C
• Refractive Index: 1.491
• CAS DataBase Reference: [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE(64723-73-5)
• EPA Substance Registry System: [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE(64723-73-5)

Safety Data

• Hazardous Substances Data: 64723-73-5(Hazardous Substances Data)

Usage

General Description

[1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE is a chemical compound with the molecular formula C14H17N. It is a yellow to brown crystalline solid that is insoluble in water and soluble in organic solvents. [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE is commonly used in the pharmaceutical and chemical industries as a reagent and intermediate. It is also used in the synthesis of various organic compounds, including pharmaceutical drugs and agrochemicals. The chemical structure of [1,3-DIMETHYL-BUT-2-EN-(E)-YLIDENE]-PHENYL-AMINE contains a butenylidene group and a phenylamine group, which are important functional groups in organic chemistry. Overall, this compound has a wide range of applications and is an important building block in the synthesis of various organic compounds.

InChI:InChI=1/C12H15N/c1-10(2)9-11(3)13-12-7-5-4-6-8-12/h4-9H,1-3H3/b13-11+

Upstream product

• 141-79-7 4-methyl-pent-3-en-2-one 
• 62-53-3 aniline 
• 1124-52-3 N-(propan-2-ylidene)aniline 

Downstream Products

• 141-79-7 4-methyl-pent-3-en-2-one 
• 62-53-3 aniline 
• 86129-88-6 N,3,3-Triphenyl-4-methyl-4-(2-methylpropenyl)-2-azetidinone 
• 64723-77-9 [1,3-Dimethyl-3-phenyl-but-(E)-ylidene]-phenyl-amine 
• 64723-79-1 N-(1,3,3,4-tetramethyl-pent-4-enylidene)-aniline 
• 64723-75-7 N-(1,3,3-trimethyl-heptylidene)-aniline 

Relevant articles and documents

Halogenated Ketenes. 38. Cycloaddition of α,β-Unsaturated Imines with Ketenes To Yield Both β- and δ-Lactams

The cycloaddition of various types of α,β-unsaturated imines with diphenyl- and dichloroketenes yields both (2 + 2) and (4 + 2) cycloaddition products, i. e., β-lactams and δ-lactams, respectively.The cycloaddition products are dependent upon substitution in the imine and the ketene.The δ-lactams derived from dichloroketene are easily dehydrochlorinated to the corresponding 2-pyridones.All of the results are consistent with a two-step cycloaddition process involving a dipolar intermediate.