205485-29-6

Basic information

• Product Name: [2-Methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-methanol
• Synonyms: [2-Methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-methanol
• CAS NO: 205485-29-6
• Molecular Weight: 246.189
• Mol File: 205485-29-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [2-Methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [2-Methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-methanol(205485-29-6)
• EPA Substance Registry System: [2-Methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-phenyl]-methanol(205485-29-6)

Safety Data

• Hazardous Substances Data: 205485-29-6(Hazardous Substances Data)

Upstream product

• 877667-30-6 2,2,2-trifluoro-1-(3-methoxyphenyl)-N-{[(4-methylphenyl)sulfonyl]oxy}ethanimine 
• 140854-00-8 2,2,2-Trifluoro-1-(3-methoxyphenyl)ethanone oxime 
• 30724-22-2 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanone 
• 2398-37-0 3-methoxyphenyl bromide 
• 205485-25-2 2-methoxy-4-<3-trifluoromethyl-3H-diazirin-3-yl>benzaldehyde 
• 154187-45-8 3-(3-Methoxyphenyl)-3-(trifluoromethyl)diaziridine 
• 205485-24-1 3-(3-methoxyphenyl)-3-(trifluoromethyl)-3H-diazirine 

Downstream Products

• 205485-30-9 3-(4-Bromomethyl-3-methoxy-phenyl)-3-trifluoromethyl-3H-diazirine 
• 290812-03-2 {(R)-2-Hydroxy-2-[2-(2-{2-[5-((3aR,6S,6aS)-2-oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-ethoxy}-ethoxy)-ethylcarbamoyl]-ethyl}-carbamic acid 2-methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-benzyl ester 
• 885477-47-4 7-tert-butoxycarbonylmethyl-6-[2-methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-benzyl]-5-oxo-3-phenyl-tetrahydro-pyrrolo[1,2-c]oxazole-6-carboxylic acid ethyl ester 
• 887973-32-2 4-tert-butoxycarbonylmethyl-5-hydroxymethyl-3-[2-methoxy-4-(3-trifluoromethyl-3H-diazirin-3-yl)-benzyl]-2-oxo-pyrrolidine-3-carboxylic acid ethyl ester 

Relevant articles and documents

Aryldiazirine-modified pyroglutamates: Photoaffinity labels for glutamate

The synthesis of an aryldiazirine-modified pyroglutamate is reported for potential application as a photoaffinity label at glutamate receptors. Detailed 13C NMR and 19F NMR spectroscopic characterisation data for these trifluoromethy

A versatile approach for functionalization of 3-aryl-3-trifluoromethyldiazirine photophor

We introduce here a novel and simple method for the carbonylation of (alkoxyphenyl)diazirine. 3-(3-Methoxyphenyl)-3-trifluoromethyldiazirine was found to be stable under a typical Friedel-Crafts reaction producing carboxaldehyde derivatives of methoxyphen