83520-63-2

Basic information

• Product Name: 2-hydroxy-5-nitrostyrene
• Synonyms: 2-hydroxy-5-nitrostyrene
• CAS NO: 83520-63-2
• Molecular Weight: 165.148
• Mol File: 83520-63-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-hydroxy-5-nitrostyrene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxy-5-nitrostyrene(83520-63-2)
• EPA Substance Registry System: 2-hydroxy-5-nitrostyrene(83520-63-2)

Safety Data

• Hazardous Substances Data: 83520-63-2(Hazardous Substances Data)

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 97-51-8 5-Nitrosalicylaldehyde 
• 280113-67-9 5-nitro-2-(prop-2-ynyloxy)benzaldehyde 
• 280113-46-4 5-nitro-2-(2-propynyloxy)styrene 

Downstream Products

• 1607446-62-7 4-(2-hydroxy-5-nitrophenyl)-1-phenylpentan-3-one 
• 1607446-63-8 2-(2-hydroxy-5-nitrophenyl)octan-3-one 
• 1607446-72-9 (E)-2-(2-hydroxy-5-nitrophenyl)-4-methylhex-4-en-3-one 
• 1607446-73-0 C₁₇H₁₈N₂O₄ 
• 1607447-02-8 N,N-dimethyl-4-(3-methyl-5-nitrobenzofuran-2-yl)aniline 
• 1607446-74-1 C₁₆H₁₅NO₅ 
• 1607447-01-7 2-(4-methoxyphenyl)-3-methyl-5-nitrobenzofuran 
• 1607446-75-2 2-(2-hydroxy-5-nitrophenyl)-1-phenylpropan-1-one 
• 860580-15-0 C₁₅H₁₃NO₄ 
• 1607446-76-3 methyl 4-(2-(2-hydroxy-5-nitrophenyl)propanoyl)benzoate 
• 1607446-77-4 1-(4-hydroxy-3-methoxyphenyl)-2-(2-hydroxy-5-nitrophenyl)propan-1-one 

Relevant articles and documents

Aryloxybenzylidene ruthenium chelates: Synthesis, structure and catalytic activity in olefin metathesis

New aryloxybenzylidene ruthenium chelates behave like a promising latent catalyst of olefin metathesis. The catalysts are characterised by substantial stability and catalytic inactivity in their dormant forms and a dramatic increase in activity after addi

3H-1,2-benzoxathiepine 2,2-dioxides: a new class of isoform-selective carbonic anhydrase inhibitors

A new chemotype with carbonic anhydrase (CA, EC 4.2.1.1) inhibitory action has been discovered, the homo-sulfocoumarins (3H-1,2-benzoxathiepine 2,2-dioxides) which have been designed considering the (sulfo)coumarins as lead molecules. An original synthetic strategy of a panel of such derivatives led to compounds with a unique inhibitory profile and very high selectivity for the inhibition of the tumour associated (CA IX/XII) over the cytosolic (CA I/II) isoforms. Although the CA inhibition mechanism with these new compounds is unknown for the moment, we hypothesize that it may be similar to that of the sulfocoumarins, i.e. hydrolysis to the corresponding sulfonic acids which thereafter anchor to the zinc-coordinated water molecule within the enzyme active site.

Aryloxybenzylidene ruthenium chelates: Synthesis, structure and catalytic activity in olefin metathesis

New aryloxybenzylidene ruthenium chelates behave like a promising latent catalyst of olefin metathesis. The catalysts are characterised by substantial stability and catalytic inactivity in their dormant forms and a dramatic increase in activity after addi