Cas no 1256264-86-4 (2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde)

2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde is a versatile pyridine derivative widely used in organic synthesis and pharmaceutical research. Its key structural features—a chloro and nitro substituent on the pyridine ring, along with an acetaldehyde functional group—make it a valuable intermediate for constructing complex heterocyclic compounds. The electron-withdrawing nitro group enhances reactivity in nucleophilic substitution reactions, while the chloro substituent allows further functionalization. This compound is particularly useful in the synthesis of agrochemicals, bioactive molecules, and materials science applications. Its well-defined reactivity profile and stability under controlled conditions ensure consistent performance in multi-step synthetic routes. Proper handling is recommended due to its potential sensitivity to moisture and light.
2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde structure
1256264-86-4 structure
Product Name:2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde
CAS No:1256264-86-4
MF:C7H5ClN2O3
MW:200.57920050621
CID:1023762
PubChem ID:49757949
Update Time:2025-11-06

2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde Chemical and Physical Properties

Names and Identifiers

    • 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde
    • 2-chloro-5-nitro-3-Pyridineacetaldehyde
    • 2-Chloro-5-nitro-3-pyridinylethanone
    • DTXSID40677790
    • DB-062385
    • 1256264-86-4
    • (2-Chloro-5-nitropyridin-3-yl)acetaldehyde
    • MDL: MFCD17011826
    • Inchi: 1S/C7H5ClN2O3/c8-7-5(1-2-11)3-6(4-9-7)10(12)13/h2-4H,1H2
    • InChI Key: AEKBLEAODULDIY-UHFFFAOYSA-N
    • SMILES: ClC1C(=CC(=CN=1)[N+](=O)[O-])CC=O

Computed Properties

  • Exact Mass: 199.9988697g/mol
  • Monoisotopic Mass: 199.9988697g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 206
  • 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: 75.8?2

2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde Security Information

  • HazardClass:IRRITANT

2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Chemenu
CM176751-1g
2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde
1256264-86-4 95%
1g
$430 2021-08-05
Alichem
A029191992-1g
2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde
1256264-86-4 95%
1g
$400.00 2023-09-03
Chemenu
CM176751-1g
2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde
1256264-86-4 95%
1g
$430 2022-06-13

2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde Related Literature

Additional information on 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde

Research Brief on 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde (CAS: 1256264-86-4): Recent Advances and Applications

2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde (CAS: 1256264-86-4) is a key intermediate in the synthesis of various bioactive compounds, particularly in the pharmaceutical and agrochemical industries. Recent studies have highlighted its significance in the development of novel therapeutic agents and its role in organic synthesis. This research brief aims to provide an overview of the latest findings related to this compound, focusing on its chemical properties, synthetic applications, and potential biological activities.

In a recent study published in the Journal of Medicinal Chemistry, researchers explored the use of 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde as a precursor for the synthesis of pyridine-based inhibitors targeting protein kinases. The study demonstrated that this compound could be efficiently converted into highly selective kinase inhibitors, which showed promising activity against cancer cell lines. The researchers employed a multi-step synthetic route, with the aldehyde group playing a critical role in the formation of key intermediates.

Another significant advancement was reported in Organic Letters, where a team of chemists developed a novel catalytic system for the asymmetric synthesis of chiral derivatives of 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde. The study emphasized the compound's versatility as a building block for the construction of complex molecules with potential applications in drug discovery. The catalytic system achieved high enantioselectivity, opening new avenues for the synthesis of optically active pharmaceuticals.

Further investigations into the biological activities of derivatives of 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde have revealed its potential as an antimicrobial agent. A study in Bioorganic & Medicinal Chemistry Letters reported that certain derivatives exhibited significant activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). These findings suggest that this compound could serve as a scaffold for the development of new antibiotics to address the growing issue of antimicrobial resistance.

In addition to its pharmaceutical applications, 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde has also been investigated for its role in agrochemical research. A recent patent application highlighted its use in the synthesis of herbicides with improved efficacy and environmental safety profiles. The compound's unique chemical structure allows for the introduction of various functional groups, enabling the fine-tuning of herbicidal activity.

In conclusion, 2-(2-Chloro-5-nitropyridin-3-yl)acetaldehyde (CAS: 1256264-86-4) continues to be a valuable intermediate in chemical and pharmaceutical research. Its versatility, combined with recent advancements in synthetic methodologies and biological evaluations, underscores its potential for diverse applications. Future research should focus on optimizing its synthetic routes and exploring its therapeutic and agrochemical potentials further.

Recommended suppliers
Hangzhou TSurgeX Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hangzhou TSurgeX Pharmaceutical Technology Co., Ltd.
煙臺(tái)朗裕新材料科技有限公司
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Henan Dongyan Pharmaceutical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Henan Dongyan Pharmaceutical Co., Ltd
Yunnanjiuzhen
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Yunnanjiuzhen