22824-20-0

Basic information

• Product Name: Benzenebutanoic acid, 2-nitro-, methyl ester
• CAS NO: 22824-20-0
• Molecular Formula: C11H13NO4
• Molecular Weight: 223.229
• Mol File: 22824-20-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenebutanoic acid, 2-nitro-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenebutanoic acid, 2-nitro-, methyl ester(22824-20-0)
• EPA Substance Registry System: Benzenebutanoic acid, 2-nitro-, methyl ester(22824-20-0)

Safety Data

• Hazardous Substances Data: 22824-20-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 67857-97-0 4-(2-nitrophenyl)-n-butyric acid 
• 88-72-2 1-methyl-2-nitrobenzene 
• 292638-85-8 acrylic acid methyl ester 
• 1701-57-1 2,3,4,5-tetrahydro-1Hbenzo[b]azepine 
• 5600-62-4 4-(4-nitrophenyl)butanoic acid 
• 609-73-4 o-nitroiodobenzene 
• 7440-66-6 zinc 
• 1821-12-1 4-Phenylbutyric acid 

Downstream Products

• 46320-17-6 4-(2-aminophenyl)butanoic acid methyl ester 
• 113849-32-4 4-(2,4-Diamino-phenyl)-butyric acid methyl ester 
• 943345-27-5 4-(2-{[5-(4-methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]amino}phenyl)butanoic acid methyl ester 
• 943345-28-6 4-(2-{[5-(4-Methoxyphenyl)-6-phenylfuro[2,3-d]pyrimidin-4-yl]amino}phenyl)butanoic acid 
• 113849-35-7 methyl 4-phenyl>butyrate 
• 113849-34-6 methyl 4-phenyl>butyrate 

Relevant articles and documents

Deconstructive di-functionalization of unstrained, benzo cyclic amines by C-N bond cleavage using a recyclable tungsten catalyst

With H2WO4 as the catalyst and H2O2 as the oxidant, we herein report a deconstructive difunctionalization of the C-N bond in unstrained, benzo cyclic amines to generate an ester group and nitro group simultaneously. The preliminary mechanistic studies suggested that the corresponding hydroxamic acid is the key intermediate for this transformation. Importantly, with the utilization of this transformation, we achieved an interesting approach for the ring contraction of quinoline to indole, an example of scaffold hopping in a hetero-aromatic system.

Novel, Cyclically Substituted Furopyrimidine Derivatives and Use Thereof

The present application relates to novel, cyclically substituted furopyrimidine derivatives, methods for their production, their use for the treatment and/or prophylaxis of diseases and their use for the production of medicinal products for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular diseases.

Process for preparation of 1,5-diaminonaphthalenes

In a process where an ortho-alkylnitrobenzene derivative and a vinyl compound as starting materials are used to prepare a 1,5-diaminonaphthalene derivative via a 4-(2-nitrobenzene)propane derivative and a 5-nitro-1-tetralone derivative, the ortho-alkylnit