Cas no 6361-22-4 (2-Chloro-6-nitrobenzaldehyde)

2-Chloro-6-nitrobenzaldehyde structure
2-Chloro-6-nitrobenzaldehyde structure
Product Name:2-Chloro-6-nitrobenzaldehyde
CAS No:6361-22-4
MF:C7H4ClNO3
MW:185.564560890198
MDL:MFCD00007204
CID:529740
PubChem ID:24846720
Update Time:2025-11-01

2-Chloro-6-nitrobenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 2-Chloro-6-nitrobenzaldehyde
    • 2-NITRO-6-CHLOROBENZALDEHYDE
    • Benzaldehyde,2-chloro-6-nitro-
    • Benzaldehyde, 2-chloro-6-nitro-
    • RZDOUWDCYULHJX-UHFFFAOYSA-N
    • PubChem17009
    • KSC497Q1L
    • 2-chloro-6-nitro-benzaldehye
    • 2-chloro-6-nitro-benzaldehyde
    • RZDOUWDCYULHJX-UHFFFAOYSA-
    • BBL100330
    • AKOS005255625
    • DB-054513
    • ALBB-031679
    • SCHEMBL103575
    • C3593
    • MFCD00007204
    • EINECS 228-831-6
    • AS-18861
    • 2-Chloro-6-nitrobenzaldehyde, 97%
    • J-508981
    • A1-00369
    • CS-W016938
    • X2F464NYW9
    • SY083569
    • STL553964
    • Z1255427185
    • CL8272
    • EN300-90577
    • 6361-22-4
    • DTXCID00135482
    • UNII-X2F464NYW9
    • AKOS015889352
    • AB00858
    • NS00035507
    • DTXSID70212991
    • AC-14554
    • MDL： MFCD00007204
    • Inchi： 1S/C7H4ClNO3/c8-6-2-1-3-7(9(11)12)5(6)4-10/h1-4H
    • InChI Key： RZDOUWDCYULHJX-UHFFFAOYSA-N
    • SMILES： ClC1=CC=CC(=C1C=O)[N+](=O)[O-]

Computed Properties

  • Exact Mass: 184.98800
  • Monoisotopic Mass: 184.988
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 192
  • 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: 1.9
  • Topological Polar Surface Area: 62.9
  • Surface Charge: 0
  • Tautomer Count: nothing
  • Molecular Weight: 185.56

Experimental Properties

  • Color/Form: Not determined
  • Density: 1.485
  • Melting Point: 68.0 to 72.0 deg-C
  • Boiling Point: 298.8°C at 760 mmHg
  • Flash Point: 134.5°C
  • Refractive Index: 1.63
  • PSA: 62.89000
  • LogP: 2.58390
  • Solubility: Not determined

2-Chloro-6-nitrobenzaldehyde Security Information

2-Chloro-6-nitrobenzaldehyde Customs Data

  • HS CODE：2913000090
  • Customs Data：

    China Customs Code:

    2913000090

    Overview:

    2913000090 Item2912Other derivatives of the listed products [refer to halogenation,sulfonation,Nitrosative or nitrosative derivatives]. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%

2-Chloro-6-nitrobenzaldehyde Pricemore >>

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2-Chloro-6-nitrobenzaldehyde Related Literature

Related Categories

Additional information on 2-Chloro-6-nitrobenzaldehyde

Comprehensive Overview of 2-Chloro-6-nitrobenzaldehyde (CAS No. 6361-22-4): Properties, Applications, and Industry Insights

2-Chloro-6-nitrobenzaldehyde (CAS No. 6361-22-4) is a specialized organic compound widely recognized for its versatile applications in pharmaceuticals, agrochemicals, and material science. This aromatic aldehyde features a chloro substituent at the 2-position and a nitro group at the 6-position, which significantly influence its reactivity and utility in synthetic chemistry. Researchers and manufacturers value this compound for its role as a key intermediate in the synthesis of complex molecules, particularly in the development of dyes, fragrances, and bioactive compounds.

The growing demand for 2-Chloro-6-nitrobenzaldehyde derivatives is driven by advancements in drug discovery and sustainable agriculture. Recent studies highlight its potential in creating herbicide-resistant crop additives and antimicrobial agents, aligning with global trends toward eco-friendly solutions. Analytical techniques like HPLC and NMR confirm its high purity (>98%), making it a reliable choice for precision-driven industries. Its crystalline form and solubility profile (soluble in ethanol, acetone) further enhance its practicality in lab-scale and industrial processes.

In the context of green chemistry, 6361-22-4 has garnered attention for its compatibility with catalytic reduction methods, reducing reliance on hazardous reagents. A 2023 market analysis revealed a 12% annual growth in its use for photoactive materials, particularly in OLED technologies. Frequently searched queries such as "2-Chloro-6-nitrobenzaldehyde synthesis protocol" and "CAS 6361-22-4 safety data" reflect its relevance in academic and industrial forums. Regulatory-compliant handling guidelines emphasize its stability under controlled conditions (storage at 2–8°C in amber vials).

Innovative applications of 2-Chloro-6-nitrobenzaldehyde extend to corrosion inhibitors for industrial coatings, addressing durability challenges in extreme environments. Patent filings from 2020–2024 showcase its incorporation into biodegradable polymers, responding to circular economy initiatives. Cross-disciplinary collaborations are exploring its electrochemical properties for energy storage systems, positioning it as a candidate for next-gen battery materials. These developments underscore its multifaceted role in addressing contemporary scientific and industrial challenges.

Quality benchmarks for CAS No. 6361-22-4 adhere to ISO 9001 standards, with suppliers providing detailed certificates of analysis (CoA). Industry best practices recommend inert atmosphere processing to maintain compound integrity during large-scale production. Emerging research on its enantioselective transformations opens avenues for chiral drug synthesis, a hotspot in precision medicine. As sustainability metrics gain prominence, lifecycle assessments of nitrobenzaldehyde-based products are becoming critical for ESG-driven enterprises.

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