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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
5 Results for "
nitrous acid
" in MedChemExpress (MCE) Product Catalog:
Products (5)
5 Results for "nitrous acid" in MCE Product Catalog:
Cat. No.: HY-W019334
CAS No.: 202842-98-6
Synonyms: 3,4-DMPP
3,4-Dimethylpyrazole phosphate (3,4-DMPP) is a nitrification inhibitor and microbial community regulator, whose activity is dose- and soil pH-dependent. 3,4-Dimethylpyrazole phosphate inhibits ammonia monooxygenase, ammonia-oxidizing bacteria, as well as ammonia-oxidizing archaea and nitrite-oxidizing bacteria. 3,4-Dimethylpyrazole phosphate alters the community composition of prokaryotes, fungi and ammonia-oxidizing bacteria. 3,4-Dimethylpyrazole phosphate reduces nitrate leaching, nitrous oxide emission and soil nitrate accumulation, and enhances nitrogen use efficiency and crop yield in agricultural production. 3,4-Dimethylpyrazole phosphate is applicable to agriculture-related research .
Cat. No.: HY-W007345
CAS No.: 53981-24-1
Synonyms: 4-Fluoro-2-hydroxyaniline
Target:
Research Areas:
2-Amino-5-fluorophenol is an isomer of aminofluorophenol and also a HONO generator. 2-Amino-5-fluorophenol reacts with nitrogen dioxide (NO2) via two pathways to form nitrous acid (HONO): hydrogen abstraction from the hydroxyl group and hydrogen abstraction from the amino group, with both the amino and hydroxyl groups participating in the reaction in the transition state .
Cat. No.: HY-W702094
CAS No.: 1330277-32-1
Cat. No.: HY-116121
CAS No.: 139427-42-2
Target:
Research Areas:
S-Nitrosohomocysteine is a compound generated by the reaction of homocysteine and nitrous acid. It has the activity of quantitative formation under different pH conditions and its stability is affected by transition metal ions. Its formation involves more powerful nitrosating agents.
Cat. No.: HY-W392912A
CAS No.: 2833-24-1
Synonyms: Methyl (2E)-4-oxopent-2-enoate
Research Areas:
Methyl trans-4-oxo-2-pentenoate (Methyl (2E)-4-oxopent-2-enoate) is a heterofunctionalized dienophile containing both ketone and ester functional groups. The enone structure within the Methyl trans-4-oxo-2-pentenoate molecule makes it a highly reactive Michael acceptor capable of regioselective conjugate addition, which is commonly used in reactions for constructing complex ring systems such as the Robinson annulation. Methyl trans-4-oxo-2-pentenoate can serve as a substrate in the synthesis of α-(alkylmethylene) butyrolactone derivatives. Methyl trans-4-oxo-2-pentenoate participates in asymmetric Diels-Alder reactions promoted by chiral palladium complexes .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
