55215-55-9

Usage

Uses

Used in Organic Synthesis:
1,4-Diiodo-2-methoxy-5-nitrobenzene is utilized as a starting material in organic synthesis, specifically for the preparation of a range of pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the development of these products.
Used as a Reagent in Chemical Reactions:
In the field of chemistry, 1,4-Diiodo-2-methoxy-5-nitrobenzene also serves as a reagent, particularly in the synthesis of heterocyclic compounds. Its role in these reactions is crucial for the formation of complex organic molecules.
Used in Pharmaceutical and Agrochemical Industries:
Given its applications in organic synthesis and as a reagent, 1,4-Diiodo-2-methoxy-5-nitrobenzene is instrumental in the pharmaceutical and agrochemical industries. It contributes to the creation of new drugs and agricultural products, enhancing their efficacy and performance.
Safety Considerations:

Upstream product

• 766-85-8 3-methoxy-1-iodobenzene 
• 335349-66-1 4-iodo-5-methoxy-2-nitroaniline 

Downstream Products

• 1427311-72-5 (R/S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethyl-1-propanol 
• 1427311-74-7 (R)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethyl-1-propyl (1S)-camphanate 
• 1427311-75-8 (S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethyl-1-propyl (1S)-camphanate 
• 1427311-76-9 (S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethyl-1-propanol 
• 1427311-53-2 6-chloro-9-(β-D-2’-deoxyribofuranosyl)-7-[(S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-7-deazapurine 
• 1427311-54-3 7-[(S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-7-deaza-2’-deoxyadenosine 
• 1427311-55-4 7-{(S)-1-[5-methoxy-4-(3-trifluoroacetamido-1-propynyl)-2-nitrophenyl]-2,2-dimethylpropyloxy}methyl-7-deaza-2'-deoxyadenosine 
• 1427311-56-5 7-{(S)-1-[4-(3-amino-1-propynyl)-5-methoxy-2-nitrophenyl]-2,2-dimethylpropyloxy}methyl-7-deaza-2‘-deoxyadenosine-5‘-triphosphate 
• 1427311-77-0 7-{(S)-1-[4-(3-amino-1-propynyl)-5-methoxy-2-nitrophenyl]-2,2-dimethylpropyloxy}methyl-7-deaza-2’-deoxyadenosine-5’-α-thiotriphosphate 
• 1427311-58-7 2-amino-6-chloro-9-(β-D-2’-deoxyribofuranosyl)-7-[(S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-7-deazapurine 
• 1427311-62-3 5-[(S)-1-(4-iodo-5-methoxy-2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-2’-deoxyuridine 
• 1427311-63-4 5-{(S)-1-[5-methoxy-4-(3-trifluoroacetamido-1-propynyl)-2-nitrophenyl]-2,2-dimethylpropyloxy}methyl-2'-deoxyuridine 

Relevant academic research and scientific papers

Method for synthesizing 1,4-diiodo-2-methoxy-5-nitrobenzene

The invention relates to the field of organic synthesis and discloses a method for synthesizing 1,4-diiodo-2-methoxy-5-nitrobenzene. The method includes the steps that firstly, 5-chloro-2-nitroaniline reacts with N-iodosuccinimide to generate 2-chloro-4-c

5-METHOXY. 3'-OH UNBLOCKED, FAST PHOTOCLEAVABLE TERMINATING NUCLEOTIDES AND METHODS FOR NUCLEIC ACID SEQUENCING

The present invention relates generally to 3'-OH unblocked nucleotides and nucleosides labeled and unlabeled with 5-methoxy-substituted nitrobenzyl-based photocleavable terminating groups for use in methods and systems related to DNA and RNA sequencing an