770-37-6

Basic information

• Product Name: 2-(benzylideneamino)ethanol
• Synonyms: 2-(benzylideneamino)ethanol
• CAS NO: 770-37-6
• Molecular Formula: C₉H₁₁NO
• Molecular Weight: 149.18974
• EINECS: 212-223-2
• Mol File: 770-37-6.mol
• Article Data: 26

Chemical Properties

• Boiling Point: 266°C at 760 mmHg
• Flash Point: 154.2°C
• Appearance: /
• Density: 0.98g/cm³
• Vapor Pressure: 0.00442mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: 2-(benzylideneamino)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzylideneamino)ethanol(770-37-6)
• EPA Substance Registry System: 2-(benzylideneamino)ethanol(770-37-6)

Safety Data

• Hazardous Substances Data: 770-37-6(Hazardous Substances Data)

Usage

Class

Aryl-alkyl amines

Appearance

Pale yellow liquid

Solubility

Soluble in water

Applications

Pharmaceuticals, agrochemicals, organic synthesis reagent

Antimicrobial properties

Potential antifungal and antimicrobial properties

Anti-inflammatory properties

Potential anti-inflammatory properties

Analgesic properties

Potential analgesic properties

InChI:InChI=1/C9H11NO/c11-7-6-10-8-9-4-2-1-3-5-9/h1-5,8,11H,6-7H2/b10-8+

Upstream product

• 100-52-7 benzaldehyde 
• 141-43-5 ethanolamine 
• 104-63-2 N-Benzylethanolamine 
• 100-51-6 benzyl alcohol 
• 100-46-9 benzylamine 

Downstream Products

• 61022-77-3 phenyl-carbamic acid-(2-benzylidenamino-ethyl ester) 
• 70509-22-7 3-methanesulfonyl-2-phenyl-oxazolidine 
• 70509-21-6 2-phenyl-3-tosyloxazolidine 
• 87537-84-6 2-Phenyl-oxazolidine-3-carboxylic acid propylamide 
• 84905-09-9 4-[(2-Hydroxy-ethylamino)-phenyl-methyl]-1,5-dimethyl-2-phenyl-1,2-dihydro-pyrazol-3-one 
• 78632-89-0 Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-azido-6-(2-{[1-phenyl-meth-(Z)-ylidene]-amino}-ethoxy)-tetrahydro-pyran-4-yl ester 
• 86709-70-8 1-<2-(Benzylideneamino)ethoxy>anthracene-9,10-dione 
• 20662-88-8 2-phenyloxazole 
• 55-21-0 benzamide 
• 100-52-7 benzaldehyde 
• 100-47-0 benzonitrile 
• 3394-32-9 2-phenyloxazolidine 
• 105427-38-1 (2-Allyloxy-ethyl)-[1-phenyl-meth-(E)-ylidene]-amine 
• 87537-82-4 2-phenyl-3-methylcarbamoyl-oxazolidine-1,3 

Relevant articles and documents

Metal array fabrication through self-assembly of Pt-complex-bound amino acids

A new type of Pt-complex-bound amino acid was synthesized by condensation of a cyclometalated Pt complex with the side-chain residue of N- and C-alkylated glutamic acid. Self-assembly of the Pt-bound lipophilic amino acid afforded a supramolecular gel in organic solvents, which comprised fibrous lamellar aggregates that supported a highly oriented Pt array.

Nitrogen-modified graphene as a metal-free carbocatalyst for the solvent-free oxidative homo- and heterocoupling of amines

In this study, graphene oxide (GO) has been prepared using Hammers’ method and the produced GO was converted to nitrogen-modified GO (NGO) using hydrothermal reaction with ammonia and hydrazine. The morphology of the product was confirmed with FESEM images and XRD, TEM, Raman, TGA, EDS, BET and FTIR analyses were employed to study the structure and properties of the product. The produced NGO has been employed as a catalyst for oxidative coupling of amines to imines. The reaction was carried out at 110?°C, using 4 wt% of catalyst (versus the used amine), oxygen gas as oxidative agent, solvent-free condition in 4?h with 80% yield. To determine the versatility of the reaction, different derivatives of amines such as benzylamine, phenyl hydrazine, aniline, ethylenediamine, ethanol amine and homoveratrylamine have been examined in this reaction and successfully converted to the related imines via heterocoupling reactions. Finally, the recyclability of the reaction was investigated and the results showed only 10% decreasing in the yield after 6 runs.

STEREOSELECTIVE PROCESS FOR PREPARING SUBSTITUTED POLYCYCLIC PYRIDONE DERIVATIVES

The present invention provides industrially suitable processes for preparing intermediates in the production of substituted polycyclic pyridone derivatives having a cap-dependent endonuclease inhibitory activity. In the process as shown below, wherein each symbol is as defined in the specification, an optically active substituted tricyclic pyridone derivative of the formula (VII) is obtained in high yield and high enantioselectivity by subjecting a compound of the formula (III) or (VI) to intramolecular cyclization with controlling stereochemistry to obtain a compound of the formula (IV) having a removable functional group on an asymmetric carbon, and then removing the functional group thereof.