112239-00-6

Basic information

• Product Name: Methyl 2-iodo-5-nitrobenzoate
• Synonyms: Methyl 2-iodo-5-nitrobenzoate;2-Iodo-5-nitro-benzoic acid Methyl ester
• CAS NO: 112239-00-6
• Molecular Formula: C₈H₆INO₄
• Molecular Weight: 307.04201
• EINECS: 604-604-1
• Mol File: 112239-00-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerated.
• CAS DataBase Reference: Methyl 2-iodo-5-nitrobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-iodo-5-nitrobenzoate(112239-00-6)
• EPA Substance Registry System: Methyl 2-iodo-5-nitrobenzoate(112239-00-6)

Safety Data

• Hazardous Substances Data: 112239-00-6(Hazardous Substances Data)

Usage

General Description

Methyl 2-iodo-5-nitrobenzoate is an organic chemical compound with the molecular formula C8H6INO4. It is a derivative of benzoic acid and is primarily used as an intermediate in the synthesis of pharmaceuticals and other complex organic molecules. It is a pale yellow solid with a high melting point, and it is sparingly soluble in water but more soluble in organic solvents. Methyl 2-iodo-5-nitrobenzoate is a versatile building block in the field of organic chemistry and is used in various research and industrial applications. It is important to handle this compound with care as it is classified as a hazardous chemical.

Upstream product

• 67-56-1 methanol 
• 19230-50-3 2-iodo-5-nitro-benzoic acid 
• 860567-09-5 2-iodo-5-nitrobenzoic acid chloride 
• 616-79-5 2-amino-5-nitro-benzoic acid 
• 88-67-5 2-Iodobenzoic acid 
• 7664-93-9 sulfuric acid 
• 1830-16-6 1-hydroxy-5-nitro-1λ³-benzo[d][1,2]iodaoxol-3(1H)-one 
• 610-97-9 o-iodo-methyl-benzoic acid 

Downstream Products

• 181376-12-5 2-iodo-5-nitrobenzamide 
• 54255-63-9 2-phenoxy-5-nitrobenzoic acid 
• 33413-97-7 2-(4-methylphenoxy)-5-nitrobenzoic acid 
• 616-71-7 2-Hydroxy-5-nitrobenzoesaeurephenylester 
• 346704-90-3 methyl 5-nitro-2-phenoxy-benzoate 
• 35486-62-5 Methyl-5-nitro-2-p-tolyloxybenzoat 
• 100038-90-2 2-(2-Carboxy-phenylamino)-5-nitro-benzoic acid methyl ester 
• 1065102-79-5 methyl 5-amino-2-iodobenzoate 
• 1417728-44-9 3-benzyl-6-nitro-2-phenylquinazolin-4(3H)-one 
• 200880-17-7 1-(2-carboxy-4-nitrophenyl)-4-nitronaphthalene 
• 200880-16-6 1-(2-carboxy-4-nitrophenyl)-2-nitronaphthalene 

Relevant articles and documents

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Synthesis and properties of microenvironment-sensitive oligonucleotides containing a small fluorophore, 3-aminobenzonitrile or 3-aminobenzoic acid

Two C-nucleosides bearing small fluorescent groups as a base were synthesized by Heck-type coupling reaction and incorporated into DNA. They exhibited environment-sensitive fluorescence and opposite solvatochromic properties. The modified DNAs containing 3-aminobenzonitrile or 3-aminobenzoic acid retained the duplexes and their fluorescence reflected the microenvironment.

Activated iododerivatives for the treatment of cancer and AIDS

A series of activated iodo-benzamide derivatives are described as antineoplastic and antiviral drug compounds. The compounds generally possess a chelating group, a thiol trapping group and an activating group. The presumptive mechanism of action in preven