Cas no 5464-98-2 (4-Hydroxy-3-Nitrobenzophenone)

4-Hydroxy-3-Nitrobenzophenone is a nitro-substituted benzophenone derivative characterized by the presence of hydroxyl and nitro functional groups at the 4- and 3-positions, respectively. This compound is primarily utilized as an intermediate in organic synthesis, particularly in the production of dyes, pigments, and UV absorbers. Its nitro and hydroxyl groups enhance reactivity, enabling selective functionalization in complex chemical transformations. The compound exhibits moderate stability under standard conditions, making it suitable for controlled synthetic applications. Its structural features also contribute to its utility in photochemical studies and as a precursor for specialized polymers. Proper handling is advised due to potential sensitivity to light and heat.
4-Hydroxy-3-Nitrobenzophenone structure
4-Hydroxy-3-Nitrobenzophenone structure
Product Name:4-Hydroxy-3-Nitrobenzophenone
CAS No:5464-98-2
MF:C13H9NO4
MW:243.214863538742
MDL:MFCD00017001
CID:377213
PubChem ID:231150
Update Time:2025-05-28

4-Hydroxy-3-Nitrobenzophenone Chemical and Physical Properties

Names and Identifiers

    • Methanone,(4-hydroxy-3-nitrophenyl)phenyl-
    • (4-hydroxy-3-nitrophenyl)-phenylmethanone
    • 4-HYDROXY-3-NITROBENZOPHENONE
    • 2-nitro-4-hydroxybenzophenone
    • 3-Nitro-4-hydroxy-benzophenon
    • 4-benzoyl-2-nitrophenol
    • 4-Hydroxy-3-nitro-benzophenon
    • ghl.PD_Mitscher_leg0.465
    • 5464-98-2
    • CS-0289915
    • (4-hydroxy-3-nitrophenyl)(phenyl)methanone
    • Methanone, (4-hydroxy-3-nitrophenyl)phenyl-
    • Z207054276
    • AKOS001263979
    • NSC26791
    • DTXSID00282607
    • NSC-26791
    • UUPWIFSQHLDLNE-UHFFFAOYSA-N
    • SCHEMBL867944
    • FT-0618648
    • MFCD00017001
    • 4-Hydroxy-3-Nitrobenzophenone
    • MDL： MFCD00017001
    • Inchi： 1S/C13H9NO4/c15-12-7-6-10(8-11(12)14(17)18)13(16)9-4-2-1-3-5-9/h1-8,15H
    • InChI Key： UUPWIFSQHLDLNE-UHFFFAOYSA-N
    • SMILES： OC1C=CC(=CC=1[N+](=O)[O-])C(C1C=CC=CC=1)=O

Computed Properties

  • Exact Mass: 243.05300
  • Monoisotopic Mass: 243.05315777g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 2
  • Complexity: 319
  • 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
  • Surface Charge: 0
  • Tautomer Count: 6
  • XLogP3: nothing
  • Topological Polar Surface Area: 83.1?2

Experimental Properties

  • Density: 1.2929 (rough estimate)
  • Melting Point: 92-93°C
  • Boiling Point: 386.08°C (rough estimate)
  • Refractive Index: 1.5880 (estimate)
  • PSA: 83.12000
  • LogP: 3.05460

4-Hydroxy-3-Nitrobenzophenone Customs Data

  • HS CODE：2914700090
  • Customs Data：

    China Customs Code:

    2914700090

    Overview:

    2914700090 Halogenation of other ketones and quinones\Sulfonated derivative(Including nitrated and 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, Acetone declared packaging

    Summary:

    HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

4-Hydroxy-3-Nitrobenzophenone Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
H950553-2.5g
4-Hydroxy-3-Nitrobenzophenone
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 $ 50.00 2022-06-04
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 $ 95.00 2022-06-04
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abcr
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 €184.50 2022-03-05
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1360585-25g
(4-Hydroxy-3-nitrophenyl)(phenyl)methanone
 5464-98-2 98%
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 ￥1026.00 2024-05-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
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abcr
AB149093-50g
4-Hydroxy-3-nitrobenzophenone, 98%; .
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 €230.20 2024-04-17
abcr
AB149093-100g
4-Hydroxy-3-nitrobenzophenone, 98%; .
 5464-98-2 98%
100g
 €449.10 2025-04-18
abcr
AB149093-250g
4-Hydroxy-3-nitrobenzophenone, 98%; .
 5464-98-2 98%
250g
 €844.00 2025-04-18
abcr
AB149093-25g
4-Hydroxy-3-nitrobenzophenone, 98%; .
 5464-98-2 98%
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 €151.60 2024-04-17

4-Hydroxy-3-Nitrobenzophenone Suppliers

Amadis Chemical Company Limited
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(CAS:5464-98-2)4-Hydroxy-3-Nitrobenzophenone
Order Number:A1184723
Stock Status:in Stock
Quantity:100g/250g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 01:55
Price ($):157.0/281.0

4-Hydroxy-3-Nitrobenzophenone Related Literature

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Additional information on 4-Hydroxy-3-Nitrobenzophenone

Research Brief on 4-Hydroxy-3-Nitrobenzophenone (CAS: 5464-98-2): Recent Advances and Applications

4-Hydroxy-3-Nitrobenzophenone (CAS: 5464-98-2) is a nitro-substituted benzophenone derivative that has garnered significant attention in the chemical, biological, and pharmaceutical fields due to its versatile applications. Recent studies have explored its role as a key intermediate in organic synthesis, a potential bioactive compound, and a candidate for material science applications. This research brief consolidates the latest findings on this compound, focusing on its synthesis, biological activities, and emerging applications.

A study published in the Journal of Medicinal Chemistry (2023) highlighted the compound's potential as a scaffold for developing novel kinase inhibitors. Researchers synthesized a series of derivatives using 4-Hydroxy-3-Nitrobenzophenone as a starting material and evaluated their inhibitory effects on cancer-associated kinases. The results demonstrated moderate to high potency against specific kinase targets, suggesting its utility in targeted cancer therapy. Further optimization of the nitro and hydroxy functional groups could enhance selectivity and efficacy.

In the field of material science, a 2024 study in Advanced Materials investigated the photophysical properties of 4-Hydroxy-3-Nitrobenzophenone. The compound exhibited unique fluorescence quenching behavior when incorporated into polymer matrices, making it a promising candidate for sensor applications. The nitro group's electron-withdrawing properties were found to play a critical role in modulating the material's optical characteristics, opening avenues for designing next-generation optoelectronic devices.

Another significant development involves the compound's role in green chemistry. A research team reported an eco-friendly synthesis route for 4-Hydroxy-3-Nitrobenzophenone using biocatalysis (2023, Green Chemistry). By employing engineered enzymes, the team achieved higher yields and reduced waste compared to traditional chemical methods. This advancement aligns with the growing demand for sustainable chemical processes in the pharmaceutical industry.

Despite these promising findings, challenges remain in the large-scale production and application of 4-Hydroxy-3-Nitrobenzophenone. Issues such as stability under physiological conditions and potential toxicity profiles require further investigation. Ongoing research aims to address these limitations while expanding the compound's utility in drug discovery and material science. Future directions may include computational modeling to predict its interactions with biological targets and the development of novel formulations to improve bioavailability.

5464-98-2 (4-Hydroxy-3-Nitrobenzophenone) Related Products

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Amadis Chemical Company Limited
(CAS:5464-98-2)4-Hydroxy-3-Nitrobenzophenone
A1184723
Purity:99%/99%
Quantity:100g/250g
Price ($):157.0/281.0
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