20876-28-2

Basic information

• Product Name: 2-METHOXY-6-NITROPHENYLACETIC ACID
• Synonyms: 2-METHOXY-6-NITROPHENYLACETIC ACID;2-(2-methoxy-6-nitrophenyl)acetic acid
• CAS NO: 20876-28-2
• Molecular Formula: C₉H₉NO₅
• Molecular Weight: 211.17
• Mol File: 20876-28-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 172 °C
• Boiling Point: 380.7±27.0 °C(Predicted)
• Appearance: /
• Density: 1.382±0.06 g/cm3(Predicted)
• PKA: 3.79±0.10(Predicted)
• CAS DataBase Reference: 2-METHOXY-6-NITROPHENYLACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHOXY-6-NITROPHENYLACETIC ACID(20876-28-2)
• EPA Substance Registry System: 2-METHOXY-6-NITROPHENYLACETIC ACID(20876-28-2)

Safety Data

• Hazardous Substances Data: 20876-28-2(Hazardous Substances Data)

Upstream product

• 4837-89-2 pyruvic acid 
• 20876-27-1 (6-methoxy-2-nitrophenyl)acetonitrile 
• 102308-58-7 (2-methoxy-6-nitro-phenyl)-acetic acid amide 
• 50-00-0 formaldehyd 
• 5460-31-1 3-nitro-o-cresol 
• 74-88-4 methyl iodide 
• 4837-88-1 6-methoxy-2-nitrotoluene 
• 95-92-1 oxalic acid diethyl ester 
• 7722-84-1 dihydrogen peroxide 
• 19689-86-2 2-nitro-6-methoxybenzyl bromide 
• 64208-72-6 2-chloromethyl-3-nitro-anisole 
• 33844-24-5 2-methoxy-6-nitro-benzoyl chloride 
• 101861-48-7 2-diazo-1-(2-methoxy-6-nitro-phenyl)-ethanone 
• 603-83-8 3-nitro-o-tolylamine 

Downstream Products

• 7699-17-4 4-methoxyindolin-2-one 
• 124832-33-3 1-(2-Methoxy-6-nitro-phenyl)-pent-4-en-2-one 
• 13402-55-6 4-Hydroxy-oxindol 
• 124832-34-4 5-Hydroxy-1-(2-methoxy-6-nitro-phenyl)-pentan-2-one 
• 124832-41-3 N-[3-Methoxy-2-(2,2,5,5-tetramethoxy-pentyl)-phenyl]-hydroxylamine 
• 124832-36-6 Carbonic acid allyl ester 1-cyano-5-(2-methoxy-6-nitro-phenyl)-4-oxo-pentyl ester 
• 124832-38-8 Carbonic acid allyl ester 1-cyano-5-(2-hydroxyamino-6-methoxy-phenyl)-4,4-dimethoxy-pentyl ester 
• 124832-37-7 Carbonic acid allyl ester 1-cyano-4,4-dimethoxy-5-(2-methoxy-6-nitro-phenyl)-pentyl ester 
• 7556-35-6 4-methoxy-1-methyl-1H-indole 
• 7699-21-0 4-methoxy-1-methyloxindole 

Relevant articles and documents

Non-nucleoside reverse transcriptase inhibitors

Compounds represented by formula I: wherein R1 is H, halogen, (C1-4)alkyl, O(C1-4)alkyl, and haloalkyl; R2 is H or (C1-4)alkyl; R3 is H or (C1-4)alkyl; R4 is (C1-4)alkyl, (C1-4)alkyl(C3-7)cycloalkyl, or (C3-7)cycloalkyl; and Q is a fused phenyl-5 or 6-membered saturated heterocycle having one to two heteroatoms selected from O and N, said Q being optionally substituted with hydroxy, or (C1-4)alkyl which in turn maybe optionally substituted with pyridinyl-N-oxide or C(O)OR wherein R is H or (C1-4)alkyl; or a salt thereof. The compounds have inhibitory activity against Wild Type, and single and double mutants strains, of HIV.

Esters and amides of substituted pyrrole acetic acids

Esters and amides of substituted pyrrole acetic acids are useful in the treatment of colonic polyps.