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1,4-Diiodo-2-methoxy-5-nitrobenzene is a chemical compound characterized by its molecular formula C7H5I2NO3. It presents itself as a yellow crystalline solid, typically available in the form of a fine powder. 1,4-Diiodo-2-methoxy-5-nitrobenzene is known for its potential applications in various chemical processes and industries.

55215-55-9

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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:

Check Digit Verification of cas no

The CAS Registry Mumber 55215-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55215-55:
(7*5)+(6*5)+(5*2)+(4*1)+(3*5)+(2*5)+(1*5)=109
109 % 10 = 9
So 55215-55-9 is a valid CAS Registry Number.

55215-55-9Relevant academic research and scientific papers

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

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Paragraph 0033-0035, (2017/08/27)

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

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Page/Page column 136; 139; 140; 141, (2013/03/28)

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

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