20941-14-4

Basic information

• Product Name: N-benzyl-1-[4-(benzyliminomethyl)phenyl]methanimine
• CAS NO: 20941-14-4
• Molecular Formula: C₂₂H₂₀N₂
• Molecular Weight: 312.4076
• Mol File: 20941-14-4.mol

Chemical Properties

• Boiling Point: 463.629°C at 760 mmHg
• Flash Point: 227.019°C
• Density: 1.006g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.573
• CAS DataBase Reference: N-benzyl-1-[4-(benzyliminomethyl)phenyl]methanimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-1-[4-(benzyliminomethyl)phenyl]methanimine(20941-14-4)
• EPA Substance Registry System: N-benzyl-1-[4-(benzyliminomethyl)phenyl]methanimine(20941-14-4)

Safety Data

• Hazardous Substances Data: 20941-14-4(Hazardous Substances Data)

Upstream product

• 623-27-8 terephthalaldehyde, 
• 100-46-9 benzylamine 

Downstream Products

• 1141739-83-4 1,4-phenylene-bis-(N-benzylaminomethanephosphonous) acid 
• 235432-96-9 Pt₂(CH₃)2(S(CH₃)2)2(C₂₂H₁₈N₂) 
• 25790-41-4 Benzyl[4-(benzylaminomethyl)benzyl]amine 

Relevant articles and documents

Addition of dimethyl phosphite to N,N'-dialkyl-and-diaryl terephthalaldimines and its stereochemistry contrary to behavior of other analogues

The addition of dimethyl phosphite to N,N'-terephthalylidene-alkyl- (or aryl-) amines resulted in new tetramethyl 1,4-phenylene-bis-(N-alkylaminomethyl)-phosphonates in moderate yields. The stereochemical behavior of these reactions was studied by NMR, de

Addition of Di-(trimethylsilyl)phosphite to N, N′-dialkyl terephthalic schiff bases: Synthesis of 1, 4-Phenylene-bis- (aminomethyl)- phosphonic acids

The addition of di-(trimethylsilyl)- phosphite to N,N′- terephthalylidene-alkyl-(or aryl-)- amines resulted in 1, 4-phenylene-bis-(N- alkylamino- methyl)-phosphonic acids in moderate yields. The stereochemical behavior of such reactions was studied, and N

Stereochemical aspects of the hypophosphorous acid addition to terephthalic schiff bases. Synthesis of new 1,4-phenylene-bis-aminomethane-bis-phosphonous acids

Terephthalic Schiff bases react with hypophosphorous acid to form 1,4-phenylene-bis-N-alkyl-aminomethanephosphonous acids in moderate yields. NMR studies demonstrated that - for several examples-this reaction led to the exclusive formation of only one dia

1,4-Phenylene-di(N-l-alanylaminomethylphosphonate) a new diaminophosphonate peptide receptor for lysine and arginine

New diaminophosphonate peptide receptor composed of two aminomethylphosphonic acid fragments attached to phenyl ring in para position was described. Intermolecular interactions between such host molecule and unprotected cationic forms of lysine and argini

The stereochemical behavior of terephthalic schiff bases in addition of dialkyl or diaryl phosphites

Addition of dialkyl (or diaryl) phosphites to N-alkyl terephthalic Schiff bases led exclusively to a meso-form but addition to N-aryl terephthalic Schiff bases depended on the substituent of the aryl group. Semi-empirical calculations were involved to fin

Binuclear doubly cyclometallated platinum-(II) and -(IV) compounds

Doubly cyclometallated binuclear platinum-(II) and -(IV) complexes, as well as their non-cyclometallated platinum(II) precursors, were prepared from the reactions of [Pt2Me4(μ-SMe2)2] with imine ligands derived from tereph

Pseudorotaxanes Formed between Secondary Dialkylammonium Salts and Crown Ethers

A very simple self-assembling system, which produces inclusion complexes with pseudorotaxane geometries, is described.The self-assembly of eight pseudorotaxanes with a range of stoichiometries - 1:1, 1:2, 2:1, and 2:2 (host:guest) - has been achieved.Thes

PHENYLENE-BIS-AMINOMETHANEPHOSPHONIC AND PHOSPHONOUS ACIDS

The studies on the synthesis of phenylene-bis-aminomethanephosphonic and phosphonous acids are reported.The title compounds were prepared in the reaction of the phenylene di-imine with dialkyl phosphite or hypophosphorous acid.Addition of the second phosp

Doppelring- und Doppelachsen-Pseudorotaxane

Keywords: Kronenether; Molekulare Erkennung; Rotaxane; Selbstorganisation