Cas no 27032-63-9 ((5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE)

(5-Chloro-pyridin-2-yl)-hydrazine is a versatile hydrazine derivative featuring a chlorinated pyridine core, offering distinct reactivity for synthetic applications. The presence of both hydrazine and chloro substituents on the pyridine ring enables its use as a key intermediate in the preparation of heterocyclic compounds, pharmaceuticals, and agrochemicals. Its electron-withdrawing chloro group enhances electrophilic substitution potential, while the hydrazine moiety facilitates condensation and cyclization reactions. This compound is particularly valuable in medicinal chemistry for constructing pyridazine and triazole scaffolds. High purity grades ensure consistent performance in nucleophilic and cross-coupling reactions. Proper handling is advised due to its reactive functional groups.
(5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE structure
27032-63-9 structure
Product Name:(5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE
CAS No:27032-63-9
MF:C5H6ClN3
MW:143.574239253998
MDL:MFCD07786313
CID:95265
PubChem ID:13590464
Update Time:2025-05-19

(5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE Chemical and Physical Properties

Names and Identifiers

    • Pyridine,5-chloro-2-hydrazinyl-
    • 5-Chloro-2-hydrazinylpyridine
    • Amidogen, oxo-
    • bioxyded’azote
    • bioxyded’azote(french)
    • mononitrogenmonoxide
    • nitric
    • nitricoxide0
    • nitricoxidetrimer
    • Nitrogenoxide(Nitricoxide)
    • (5-Chloro-pyridin-2-yl)-hydrazine
    • (5-chloropyridin-2-yl)hydrazine
    • 1-(5-chloropyridin-2-yl)hydrazine
    • 5-Chloro-2-hydrazinopyridine
    • 2-hydrazino-5-chloropyridine
    • 3-chloro-6-hydrazinopyridine
    • 5-chloro-2-pyridylhydrazine
    • chlorohydrazinopyridine
    • (5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE 5193-03-3
    • FT-0681035
    • AM84861
    • BCP15596
    • CS-W005325
    • SB75435
    • EN300-111786
    • DTXSID00544535
    • J-517307
    • MFCD07786313
    • UXJYFOOFLZGBEK-UHFFFAOYSA-N
    • 27032-63-9
    • 5-Chloro-2-hydrazinopyridine;5-Chloro-2-hydrazinylpyridine
    • GA-0724
    • AKOS000112929
    • SCHEMBL1432907
    • SY045855
    • A877040
    • 2(1H)-Pyridinone, 5-chloro-, hydrazone
    • (5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE
    • MDL: MFCD07786313
    • Inchi: 1S/C5H6ClN3/c6-4-1-2-5(9-7)8-3-4/h1-3H,7H2,(H,8,9)
    • InChI Key: UXJYFOOFLZGBEK-UHFFFAOYSA-N
    • SMILES: ClC1=CN=C(C=C1)NN

Computed Properties

  • Exact Mass: 143.02500
  • Monoisotopic Mass: 143.0250249g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 88.3
  • 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: 1
  • Topological Polar Surface Area: 50.9?2

Experimental Properties

  • Color/Form: No data available
  • Density: 1.418
  • Melting Point: 127-128
  • Boiling Point: 288°C at 760 mmHg
  • Flash Point: 128°C
  • PSA: 50.94000
  • LogP: 1.79390
  • pka: 9.00±0.70(Predicted)

(5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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(5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE Production Method

(5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE Related Literature

Additional information on (5-CHLORO-PYRIDIN-2-YL)-HYDRAZINE

5-Chloropyridin-2-yl Hydrazine (CAS No. 27032-63-9): A Comprehensive Overview

The compound 5-chloropyridin-2-yl hydrazine (CAS No. 27032-63-9) is a heterocyclic organic compound that has garnered significant attention in the fields of organic chemistry, pharmacology, and material science. This compound, characterized by its pyridine ring substituted with a chlorine atom at the 5-position and a hydrazine group at the 2-position, exhibits unique chemical properties that make it a valuable tool in various research and industrial applications.

5-Chloropyridin-2-yl hydrazine is widely recognized for its role as a versatile building block in organic synthesis. Its ability to participate in diverse chemical reactions, such as nucleophilic aromatic substitution and condensation reactions, has made it an essential intermediate in the construction of complex molecular architectures. Recent studies have highlighted its potential in the development of novel pharmaceutical agents, particularly in the design of kinase inhibitors and anti-inflammatory drugs.

The synthesis of 5-chloropyridin-2-yl hydrazine typically involves the reaction of 5-chloropyridine with hydrazine under specific conditions. This process is optimized to ensure high yield and purity, which are critical for its application in downstream processes. Researchers have explored various catalytic systems and reaction conditions to enhance the efficiency of this synthesis, contributing to the broader understanding of hydrazine chemistry.

In terms of applications, 5-chloropyridin-2-yl hydrazine has found utility in the development of coordination polymers and metalloorganic frameworks (MOFs). Its ability to act as a ligand for transition metals has led to the creation of materials with exceptional catalytic activity and selectivity. Recent advancements in this area have demonstrated its potential in catalytic hydrogenation and carbon dioxide capture, underscoring its importance in sustainable chemistry.

Moreover, 5-chloropyridin-2-yl hydrazine has been employed as a precursor for the synthesis of bioactive compounds. Its role in medicinal chemistry is particularly notable, as it serves as a scaffold for designing molecules with anti-cancer, anti-bacterial, and anti-viral properties. For instance, derivatives of this compound have shown promise in inhibiting key enzymes associated with neurodegenerative diseases such as Alzheimer's and Parkinson's.

The toxicological profile of 5-chloropyridin-2-yl hydrazine is another area of active research. While it is generally considered non-toxic under normal handling conditions, studies are ongoing to evaluate its long-term effects on human health and the environment. These investigations are crucial for ensuring safe handling practices and regulatory compliance in industrial settings.

In conclusion, 5-chloropyridin-2-yl hydrazine (CAS No. 27032-63-9) stands out as a multifaceted compound with applications spanning organic synthesis, materials science, and pharmacology. Its unique chemical properties and versatility continue to drive innovation across various disciplines. As research progresses, it is anticipated that this compound will play an even more pivotal role in addressing challenges in drug discovery and sustainable chemical processes.

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