92567-07-2

Basic information

• Product Name: Benzene, 1-(diazidomethyl)-4-methoxy-
• CAS NO: 92567-07-2
• Molecular Formula: C8H8N6O
• Molecular Weight: 204.191
• Mol File: 92567-07-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(diazidomethyl)-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(diazidomethyl)-4-methoxy-(92567-07-2)
• EPA Substance Registry System: Benzene, 1-(diazidomethyl)-4-methoxy-(92567-07-2)

Safety Data

• Hazardous Substances Data: 92567-07-2(Hazardous Substances Data)

Upstream product

• 150935-09-4 C₈H₈N₃O⁽¹⁺⁾ 

Downstream Products

• 150723-08-3 1-[Azido-(2,2,2-trifluoro-ethylsulfanyl)-methyl]-4-methoxy-benzene 
• 150935-09-4 C₈H₈N₃O⁽¹⁺⁾ 
• 123-11-5 4-methoxy-benzaldehyde 
• 1591950-66-1 methyl 3-azido-3-(4-methoxyphenyl)propanoate 
• 1591950-60-5 3-azido-3-(4-methoxyphenyl)-1-phenylpropan-1-one 
• 1591950-58-1 1-(1-azido-3-methylbut-3-en-1-yl)-4-methoxybenzene 
• 70978-37-9 1-(azidomethyl)-4-methoxybenzene 
• 874-90-8 4-methoxybenzonitrile 
• 150723-10-7 1-Methoxy-4-[(2,2,2-trifluoro-ethoxy)-(2,2,2-trifluoro-ethylsulfanyl)-methyl]-benzene 
• 5470-34-8 4-methoxyformanilide 
• 150723-09-4 1-[Bis-(2,2,2-trifluoro-ethoxy)-methyl]-4-methoxy-benzene 

Relevant articles and documents

Spontaneous cleavage of gem-diazides: A comparison of the effects of α-azido and other electron-donating groups on the kinetic and thermodynamic stability of benzyl and alkyl carbocations in aqueous solution

The solvolysis reactions of ring-substituted benzylic and 1-propyl gem-diazides in water proceed by a stepwise mechanism through α-azido carbocation intermediates, which are captured by water to give the corresponding aldehyde as the sole detectable produ

Kinetic and thermodynamic stability of α-azidobenzyl carbocations: Putative intermediates in the Schmidt reaction

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