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2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione is a chemical compound characterized by a molecular formula of C10H8N2O4. It is a yellow crystalline powder with a phthalazine-1,4-dione ring structure, featuring two methyl groups and a nitro group attached. 2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione is known for its unique reactivity and structural properties, which have made it a valuable component in the synthesis of various pharmaceuticals and organic compounds. Additionally, it has demonstrated some biological activity, suggesting its potential as a building block in drug discovery and development. However, due to its potential health and environmental risks, it is crucial to handle 2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione with caution.

858243-19-3

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858243-19-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure and reactivity make it a valuable component in the development of new drugs.
Used in Organic Compound Synthesis:
2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione is also used as a building block in the synthesis of a range of organic compounds. Its structural properties allow for the creation of diverse molecules with potential applications in various industries.
Used in Drug Discovery and Development:
2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione is used as a potential lead compound in drug discovery and development. Its demonstrated biological activity suggests that it could be a promising starting point for the creation of new therapeutic agents.
Used in Research and Development:
In the field of research and development, 2,3-dimethyl-5-nitro-2,3-dihydro-phthalazine-1,4-dione is used as a model compound to study the effects of its structural features on reactivity and biological activity. This can provide insights into the design of new compounds with improved properties.

Check Digit Verification of cas no

The CAS Registry Mumber 858243-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,2,4 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 858243-19:
(8*8)+(7*5)+(6*8)+(5*2)+(4*4)+(3*3)+(2*1)+(1*9)=193
193 % 10 = 3
So 858243-19-3 is a valid CAS Registry Number.

858243-19-3Relevant academic research and scientific papers

Implementation of a combinatorial cleavage and deprotection scheme. 1. Synthesis of phthalhydrazide libraries

Nielsen, John,Rasmussen, Palle H.

, p. 3351 - 3354 (2007/10/03)

Phthalhydrazide libraries are synthesized in solution from substituted hydrazines and phthalimides in several different library formats including single compounds, indexed sub-libraries and a full library. When carried out during solid-phase synthesis, this combinatorial cleavage and deprotection scheme offers the possibility for generating a diverse library of substituted phthalhydrazides. Copyright

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