117909-26-9

Basic information

• Product Name: 2-(P-TOLYLIMINO-METHYL)-PHENOL
• Synonyms: 2-(P-TOLYLIMINO-METHYL)-PHENOL;(E)-2-((p-Tolylimino)methyl)phenol
• CAS NO: 117909-26-9
• Molecular Formula: C₁₄H₁₃NO
• Molecular Weight: 211.26
• Mol File: 117909-26-9.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(P-TOLYLIMINO-METHYL)-PHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(P-TOLYLIMINO-METHYL)-PHENOL(117909-26-9)
• EPA Substance Registry System: 2-(P-TOLYLIMINO-METHYL)-PHENOL(117909-26-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 117909-26-9(Hazardous Substances Data)

Upstream product

• 89-95-2 2-methyl-benzyl alcohol 
• 106-49-0 p-toluidine 
• 53565-66-5 6-[1-p-Tolylamino-meth-(Z)-ylidene]-cyclohexa-2,4-dienone 
• 90-02-8 salicylaldehyde 
• 53565-66-5 6-[1-p-Tolylamino-meth-(Z)-ylidene]-cyclohexa-2,4-dienone 

Downstream Products

• 51891-99-7 3,4-dihydro-3-(4-methylphenyl)-2H-benz[e]-1,3-oxazine 
• 1222170-21-9 4-(4-methylphenyl)-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-thione 
• 99779-33-6 4-(4-methylphenyl)-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-one 
• 99779-28-9 2-chloro-N-(2-hydroxybenzyl)-N-(4-methylphenyl)acetamide 
• 14674-88-5 2-((p-toluidino)methyl)phenol 
• 1207178-22-0 2-(4-nitrophenyl)-3-m-tolyl-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 1207178-35-5 2-(4-nitrophenyl)-3-p-tolyl-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 1207178-27-5 2-(2-nitrophenyl)-3-p-tolyl-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 1207178-30-0 2-(3-nitrophenyl)-3-p-tolyl-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 127143-02-6 3-(2-Hydroxy-phenyl)-1-oxo-2-p-tolyl-1,2-dihydro-isoquinoline-4-carboxylic acid 

Relevant articles and documents

Synthesis of novel Schiff bases using green chemistry techniques; antimicrobial, antioxidant, antiurease activity screening and molecular docking studies

Schiff base derivatives were synthesized in this study via conventional, microwave irradiation and ultrasound sonication methods. Optimization conditions were examined for several parameter such as solvent, reaction time and yield. After determining the o

Synthesis and biological activity of some 3-aryl-3,4-dihydro-2h-benz[e]-1, 3-oxazines/6-bromo-3-aryl-3,4-dihydro-2h-benz[e]-1,3-oxazines

N-(2-Hydroxy)-benzyl-arylamine (1) gives substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines/6-bromo-3-aryl-3,4-dihydro-2H-benz[e] -1,3-oxazines (2) on cyclization with formaldehyde in methanol within 0.5-1.0 h at 65-68 C in excellent yields. Th

Synthesis of phenylthallium(III) dichloride and diphenylthallium(III) chloride complexes with bidentate Schiff base ligands: A photoelectron spectroscopic study

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