860567-09-5

Basic information

• Product Name: 2-iodo-5-nitrobenzoic acid chloride
• Synonyms: 2-iodo-5-nitrobenzoic acid chloride
• CAS NO: 860567-09-5
• Molecular Weight: 311.463
• Mol File: 860567-09-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-iodo-5-nitrobenzoic acid chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-iodo-5-nitrobenzoic acid chloride(860567-09-5)
• EPA Substance Registry System: 2-iodo-5-nitrobenzoic acid chloride(860567-09-5)

Safety Data

• Hazardous Substances Data: 860567-09-5(Hazardous Substances Data)

Upstream product

• 88-67-5 2-Iodobenzoic acid 
• 616-79-5 2-amino-5-nitro-benzoic acid 
• 19230-50-3 2-iodo-5-nitro-benzoic acid 

Downstream Products

• 1065102-79-5 methyl 5-amino-2-iodobenzoate 
• 112239-00-6 methyl 2-iodo-5-nitrobenzoate 
• 37471-18-4 4-amino-2-(4-nitrophenyl)quinazoline 
• 1408314-34-0 (1Z,3E)-3-[iodo(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)methylidene]-N-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-6-nitro-2-benzofuran-1(3H)-imine 
• 1408314-33-9 C₅₀H₅₂N₂O₁₆ 
• 1351632-85-3 9-ethyl-9H-carbazol-3-yl 2-iodo-5-nitrobenzoate 
• 1262204-01-2 N-ethyl-N-(9-ethyl-9H-carbazol-3-yl)-2-iodo-5-nitrobenzamide 
• 1262204-20-5 N-ethyl-N-(9-ethyl-1,4-dimethyl-9H-carbazol-3-yl)-2-iodo-5-nitrobenzamide 
• 250684-76-5 2-iodo-5-nitro-benzylamine 
• 101971-72-6 N-(4'-methoxyphenyl)-3-nitrobenzamide 

Relevant articles and documents

2-Iodo-N-isopropyl-5-methoxybenzamide as a highly reactive and environmentally benign catalyst for alcohol oxidation

Several N-isopropyliodobenzamides were evaluated as catalysts for the oxidation of benzhydrol to benzophenone in the presence of Oxone (2KHSO5·KHSO4·K2SO4) as a co-oxidant at room temperature. A study on the substituent effect of the benzene ring of N-isopropyl-2-iodobenzamide on the oxidation revealed that its reactivity increased in the following order of substitution: 5-NO2 2Me, 3-OMe 5-OAc 5-Cl H, 4-OMe 5-Me 5-OMe. The oxidation of various benzylic and aliphatic alcohols using a catalytic amount of the most reactive 5-methoxy derivative successfully resulted in moderate to excellent yields of the corresponding carbonyl compounds. The high reactivity of the 5-methoxy derivative at room temperature is a result of the rapid generation of the pentavalent species from the trivalent species during the reaction. 5-Methoxy-2-iodobenzamide would be an efficient and environmentally benign catalyst for the oxidation of alcohols, especially benzylic alcohols.

Compounds and compositions for use as alkylating agent sensors and methods of use thereof

This invention provides compound having a structure of Formula I: Uses of such compounds and compositions comprising the compounds as alkylating agent sensors.

SUBSTITUTED [(PHENYLETHANOYL)AMINO] BENZAMIDES AND THE USE THEREOF IN THE TREATMENT OF INFLAMMATORY AND CARDIO-VASCULAR DISEASES

The invention relates to substituted [(phenylethanoyl)amino] benzamides and to methods for the production thereof in addition to the use thereof in the production of medicaments for the treatment of and/or prophylaxis of illnesses, particularly inflammatory diseases such as diseases of the skin, respiratory passages and cardio-vascular diseases such as arteriosclerosis and coronary heart diseases.