10319-01-4

Basic information

• Product Name: 2-methyl-6-{[(2-{[(E)-(5-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}ethyl)amino]methylidene}cyclohexa-2,4-dien-1-one
• CAS NO: 10319-01-4
• Molecular Formula: C₁₈H₂₀N₂O₂
• Molecular Weight: 296.3636
• Mol File: 10319-01-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 506.9°C at 760 mmHg
• Flash Point: 182.5°C
• Density: 1.242g/cm³
• Vapor Pressure: 2.13E-10mmHg at 25°C
• Refractive Index: 1.681
• CAS DataBase Reference: 2-methyl-6-{[(2-{[(E)-(5-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}ethyl)amino]methylidene}cyclohexa-2,4-dien-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-6-{[(2-{[(E)-(5-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}ethyl)amino]methylidene}cyclohexa-2,4-dien-1-one(10319-01-4)
• EPA Substance Registry System: 2-methyl-6-{[(2-{[(E)-(5-methyl-6-oxocyclohexa-2,4-dien-1-ylidene)methyl]amino}ethyl)amino]methylidene}cyclohexa-2,4-dien-1-one(10319-01-4)

Safety Data

• Hazardous Substances Data: 10319-01-4(Hazardous Substances Data)

Upstream product

• 824-42-0 2-methoxy-3-methylbenzaldehyde 
• 107-15-3 ethylenediamine 

Relevant articles and documents

Oxovanadium(V) complexes with schiff base Ligands: Synthesis, Structure, and catalytic property

The reaction of [VO(acac)2] with N,N-ethylenebis(3-ethoxysalicylideneimine) (H2L1) and N,N-ethylenebis(3-methylsalicylideneimine) (H2L2), respectively, in methanol, affords two new oxovanadium(V) complexes, [VOL1]H2O (1) and [VOL2] (2). Both complexes hav

Syntheses of the Carotane-type Terpenoids (+)-Schisanwilsonene A and (+)-Tormesol via a Two-Stage Approach

Stereoselective syntheses of terpenoids in a more efficient manner have been a long-term pursuit for synthetic chemists. Herein we describe the two-step, enantiospecific and protecting-group-free synthesis of (+)-schisanwilsonene A from a carotane compound, which was produced in E. coli. We also completed the first enantiomeric synthesis of (+)-tormesol in five steps. The two-stage strategy offers a step- and redox-economical approach to prepare terpene natural products and their analogues.