13533-12-5

Usage

Uses

Used in Organic Synthesis:
Nitrosochloromethane is utilized as a key intermediate in the production of various chemical compounds. Its reactivity allows for its incorporation into a wide range of organic synthesis processes, making it a valuable compound in the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, nitrosochloromethane may be employed as a building block for the synthesis of pharmaceutical compounds. Its unique structure and reactivity enable the creation of novel drug candidates with potential therapeutic applications.
Used in Chemical Research:
Due to its reactivity and structural characteristics, nitrosochloromethane is also used in chemical research to study reaction mechanisms, explore new synthetic pathways, and develop innovative chemical processes.
Used in Environmental Monitoring:
Nitrosochloromethane's potential hazards highlight the need for its monitoring in industrial settings. It is used in environmental monitoring applications to ensure that its levels are kept within safe limits, thereby protecting workers and the environment from its toxic effects.

Upstream product

• 623-27-8 terephthalaldehyde, 
• 69386-99-8 terephthalaldehyde oxime 

Downstream Products

• 287398-43-0 C₂₄H₄₀N₂O₄Si₄ 
• 1047-63-8 1,4-bis-(2-benzimidazolyl)benzene 
• 195394-94-6 1,4-bis(cyanooximinomethyl)benzene 
• 3729-06-4 1,4-bis-(5-phenyl-4,5-dihydroxazole-3-yl)benzene 
• 1402043-64-4 1,4-bis-(4,5-dihydro-5-isoxazol-3-yl ethyl ether)benzene 
• 1402043-67-7 1,4-bis-(4,5-dihydro-5-isoxazolecarbonitrie-3-yl)benzene 
• 3729-34-8 terephthalobis(nitrile N-oxide) 
• 1204591-34-3 1,4-bis(4-nitrofuroxan-3-yl)benzene 
• 1204591-31-0 1,4-bis(3-nitrofuroxan-4-yl)benzene 
• 20155-72-0 octa-N-ethyl-4,5,4',5'-tetrahydro-3,3'-p-phenylene-bis-isoxazole-4,5-diamine 

Relevant academic research and scientific papers

One-pot synthesis of precise polyisoxazoles by click polymerization: Copper (I)-catalyzed 1,3-dipolar cycloaddition of nitrile oxides with alkynes

This article reports a new one-pot method for polymer preparation, which involves double click chemistry. In one pot, two click reactions take place sequentially by adding the reactants step by step. The first click reaction is to produce the monomer for

Preparation of novel Di-isoxazolines using bis(nitrile oxide) 1,3-dipolar cycloaddition methodology

A general method for the synthesis of novel di-isoxazolines through a 1,3-dipolar cycloaddition reaction of in situ prepared bis (nitrile oxides) of terephthaldehyde and various olefins is described. The reactions are regiospecific and give high yields of

Synthesis of 1,3- and 1,4-bis(3-nitrofurazan-4-yl)benzenes and isomeric 1,3- and 1,4-bis[3(4)-nitrofuroxan-4(3)-yl]benzenes

The 1,3- and 1,4-bis(3-nitrofurazan-4-yl)benzenes have been synthesized by dehydration of 1,3- and 1,4-bis(2-aminoglyoximo- 1-yl)benzenes followed by oxidation of amino groups. The 1,3- and 1,4-bis(3-nitrofuroxan-4-yl)benzenes have been prepared by nitroz

Multiple Cycloadditive macrocyclization: An Efficient Method for Crown Ether-Type Cyclophanes, Bis-Calix[4]arenes and Silamacrocycles

Macrocycles constitute a broad spectrum of compounds, which play a significant role in host-guest supramolecular chemistry. We have rationally designed an efficient novel synthetic method to synthesize different types of artificial receptive macrocycles containing isoxazoline or isoxazole ring systems. This method involves multiple (double, triple or quadrupole) cycloadditions between bifunctional dipoles and bifunctional dipolarophiles. We have presented our synthetic results to show the ease with which this one-pot synthetic method can be extended to synthesize different types of macrocycles such as cyclophanes, bis-calix[4]arenes and silamacrocycles. Hence, with appropriate combination of bifunctional dipoles and bifunctional dipolarophiles, the ring size of macrocycles could be controlled. This multiple cycloadditive macrocyclization will be a useful arsenal for the synthesis of various macrocycles.