Cas no 1001755-69-6 (3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide)

3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide is a specialized heterocyclic compound featuring a pyrazole core functionalized with a nitro group and a hydrazide side chain. This structure imparts unique reactivity, making it valuable in synthetic chemistry, particularly as an intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of both nitro and hydrazide functionalities allows for versatile transformations, including condensation and cyclization reactions. Its well-defined molecular architecture ensures consistent performance in complex synthetic pathways. The compound is typically characterized by high purity and stability under standard handling conditions, making it a reliable choice for research and industrial applications requiring precise chemical modifications.
3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide structure
1001755-69-6 structure
Product Name:3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide
CAS No:1001755-69-6
MF:C7H11N5O3
MW:213.193940401077
MDL:MFCD03423238
CID:3058097
PubChem ID:7021004
Update Time:2025-05-21

3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide Chemical and Physical Properties

Names and Identifiers

    • 3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanehydrazide
    • AKOS B015388
    • ART-CHEM-BB B015388
    • 3-(5-methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide
    • 3-(5-METHYL-3-NITRO-PYRAZOL-1-YL)-PROPIONIC ACID HYDRAZIDE
    • H33659
    • AKOS015922243
    • LS-07053
    • MFCD03423238
    • 1001755-69-6
    • BBL038503
    • ALBB-022823
    • EN300-228842
    • AKOS000305687
    • 1H-pyrazole-1-propanoic acid, 5-methyl-3-nitro-, hydrazide
    • STK312163
    • 3-(5-methyl-3-nitropyrazol-1-yl)propanehydrazide
    • 3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide
    • MDL： MFCD03423238
    • Inchi： 1S/C7H11N5O3/c1-5-4-6(12(14)15)10-11(5)3-2-7(13)9-8/h4H,2-3,8H2,1H3,(H,9,13)
    • InChI Key： LGCXEHYTSGHDNF-UHFFFAOYSA-N
    • SMILES： O=C(CCN1C(C)=CC([N+](=O)[O-])=N1)NN

Computed Properties

  • Exact Mass: 213.08618923Da
  • Monoisotopic Mass: 213.08618923Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 5
  • Complexity: 254
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.8
  • Topological Polar Surface Area: 119?2

3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide Pricemore >>

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3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide Related Literature

Additional information on 3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide

3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide: A Comprehensive Overview

3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide, also known by its CAS registry number CAS No. 1001755-69-6, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound has garnered attention due to its unique structural properties and potential applications in drug development and materials science. In this article, we will delve into the structural characteristics, synthesis methods, and recent advancements in understanding its properties and applications.

The molecular structure of 3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide is characterized by a pyrazole ring substituted with a methyl group at position 5 and a nitro group at position 3. The hydrazide group attached to the pyrazole ring introduces additional functional diversity, making this compound a versatile building block for various chemical transformations. The presence of the nitro group imparts strong electron-withdrawing effects, which can influence the electronic properties of the molecule, making it suitable for applications in electrochemistry and catalysis.

Recent studies have focused on the synthesis of this compound through various routes, including microwave-assisted synthesis and enzymatic catalysis. These methods not only enhance the efficiency of production but also align with the principles of green chemistry by minimizing waste and reducing energy consumption. For instance, researchers have reported the use of microwave irradiation to facilitate the condensation reaction between hydrazine derivatives and substituted pyrazoles, leading to high yields of 3-(5-Methyl-3-nitro-1H-pyrazol-1-yl)propanohydrazide.

In terms of applications, 3-(5-Methyl-3-nitro-1H-pyrazol-1-yL)propanohydrazide has shown promise in the field of medicinal chemistry. Its ability to act as a scaffold for bioactive molecules has been explored in several studies. For example, recent research has demonstrated its potential as an anti-inflammatory agent due to its ability to inhibit key enzymes involved in inflammatory pathways. Additionally, this compound has been investigated for its role in anticancer drug design, where its ability to target specific oncogenic pathways has been highlighted.

The versatility of this compound extends beyond pharmacology into materials science. Its unique electronic properties make it a candidate for use in organic electronics, particularly in the development of conductive polymers and semiconducting materials. Recent advancements in this area have leveraged the nitro group's electron-withdrawing effects to enhance the charge transport properties of materials incorporating 3-(5-Methyl-CAS No. 1001755_69_6.

In conclusion, 3-(5-Methyl-CAS No. 1001755_69_6) represents a multifaceted compound with diverse applications across various scientific domains. Ongoing research continues to uncover new insights into its properties and potential uses, underscoring its importance as a valuable tool in modern chemistry.

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