Cas no 1693-39-6 (N-(4-hydroxyphenyl)formamide)

N-(4-Hydroxyphenyl)formamide, also known as 4-hydroxyformanilide, is a versatile organic compound with the molecular formula C7H7NO2. It features both a hydroxyl group (-OH) and a formamide group (-NHCHO) attached to a benzene ring, making it a valuable intermediate in organic synthesis. This compound exhibits excellent reactivity in condensation and substitution reactions, enabling its use in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its hydroxyl group enhances solubility in polar solvents, facilitating purification and downstream processing. Additionally, N-(4-hydroxyphenyl)formamide serves as a precursor for synthesizing dyes, antioxidants, and bioactive molecules. Its stability under controlled conditions and high purity make it a reliable choice for research and industrial applications.
N-(4-hydroxyphenyl)formamide structure
N-(4-hydroxyphenyl)formamide structure
Product Name:N-(4-hydroxyphenyl)formamide
CAS No:1693-39-6
MF:C7H7NO2
MW:137.135981798172
CID:217671
PubChem ID:292510
Update Time:2025-11-01

N-(4-hydroxyphenyl)formamide Chemical and Physical Properties

Names and Identifiers

    • Formamide,N-(4-hydroxyphenyl)-
    • N-(4-hydroxyphenyl)formamide
    • 4-formaminophenol
    • 4-hydroxyformanilide
    • hydroxy-4 formanilide
    • N-formyl-4-hydroxyaniline
    • 4-FORMAMIDOPHENOL
    • 4'-HYDROXYFORMANILIDE
    • 4-HYDROXYPHENYLFORMAMIDE
    • N-(4-HYDROXYPHENYL)-FORMAMIDE
    • AKOS008996653
    • N-(4-hydroxyphenyl) carboxamide
    • Z87002541
    • NSC-158320
    • SCHEMBL1318230
    • DTXSID10303433
    • AB01330331-02
    • NCGC00336351-01
    • CS-0220976
    • BAA69339
    • EN300-08040
    • 1693-39-6
    • NSC158320
    • Inchi: 1S/C7H7NO2/c9-5-8-6-1-3-7(10)4-2-6/h1-5,10H,(H,8,9)
    • InChI Key: LHMWHZXZMMLYKI-UHFFFAOYSA-N
    • SMILES: OC1C=CC(=CC=1)NC=O

Computed Properties

  • Exact Mass: 137.04800
  • Monoisotopic Mass: 137.047678466g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 108
  • 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: 1.1
  • Topological Polar Surface Area: 49.3?2

Experimental Properties

  • Density: 1.3±0.1 g/cm3
  • Melting Point: 144-146 °C
  • Boiling Point: 374.9±25.0 °C at 760 mmHg
  • Flash Point: 180.6±23.2 °C
  • PSA: 49.33000
  • LogP: 1.66940
  • Vapor Pressure: 0.0±0.9 mmHg at 25°C

N-(4-hydroxyphenyl)formamide Security Information

N-(4-hydroxyphenyl)formamide Customs Data

  • HS CODE:2924299090
  • Customs Data:

    China Customs Code:

    2924299090

    Overview:

    2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

N-(4-hydroxyphenyl)formamide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
C103065-10mg
N-(4-hydroxyphenyl)formamide
1693-39-6
10mg
$ 50.00 2022-06-06
TRC
C103065-50mg
N-(4-hydroxyphenyl)formamide
1693-39-6
50mg
$ 70.00 2022-06-06
TRC
C103065-100mg
N-(4-hydroxyphenyl)formamide
1693-39-6
100mg
$ 115.00 2022-06-06
Aaron
AR007BBL-50mg
4-Hydroxyphenylformamide
1693-39-6 95%
50mg
$83.00 2025-01-23
Aaron
AR007BBL-100mg
4-Hydroxyphenylformamide
1693-39-6 95%
100mg
$116.00 2025-01-23
Aaron
AR007BBL-250mg
4-Hydroxyphenylformamide
1693-39-6 95%
250mg
$152.00 2025-01-23
Aaron
AR007BBL-500mg
4-Hydroxyphenylformamide
1693-39-6 95%
500mg
$266.00 2025-01-23
Aaron
AR007BBL-1g
4-Hydroxyphenylformamide
1693-39-6 95%
1g
$377.00 2025-01-23
Aaron
AR007BBL-2.5g
4-Hydroxyphenylformamide
1693-39-6 95%
2.5g
$717.00 2025-01-23
Aaron
AR007BBL-5g
4-hydroxyphenylformamide
1693-39-6 95%
5g
$1047.00 2023-12-15

Additional information on N-(4-hydroxyphenyl)formamide

Recent Advances in the Study of N-(4-hydroxyphenyl)formamide (CAS: 1693-39-6) in Chemical Biology and Pharmaceutical Research

N-(4-hydroxyphenyl)formamide (CAS: 1693-39-6) is a compound of significant interest in chemical biology and pharmaceutical research due to its versatile applications in drug synthesis and biological activity modulation. Recent studies have explored its potential as a key intermediate in the development of novel therapeutic agents, particularly in oncology and anti-inflammatory therapies. This research brief synthesizes the latest findings on this compound, highlighting its chemical properties, biological activities, and emerging applications in drug discovery.

One of the most notable advancements in the study of N-(4-hydroxyphenyl)formamide is its role as a precursor in the synthesis of paracetamol (acetaminophen), a widely used analgesic and antipyretic drug. Researchers have optimized the synthetic pathways involving this compound to improve yield and reduce environmental impact. A 2023 study published in the Journal of Medicinal Chemistry demonstrated a green chemistry approach utilizing N-(4-hydroxyphenyl)formamide, achieving a 92% yield with minimal waste generation. This development underscores the compound's importance in sustainable pharmaceutical manufacturing.

Beyond its role in paracetamol synthesis, N-(4-hydroxyphenyl)formamide has shown promising biological activities in its own right. Recent in vitro studies have revealed its potential as an antioxidant and anti-inflammatory agent. A 2024 paper in Bioorganic & Medicinal Chemistry Letters reported that derivatives of N-(4-hydroxyphenyl)formamide exhibited significant inhibition of reactive oxygen species (ROS) in human cell lines, suggesting potential applications in treating oxidative stress-related disorders. The study identified specific structural modifications that enhanced this activity while maintaining low cytotoxicity.

In cancer research, N-(4-hydroxyphenyl)formamide has emerged as a scaffold for developing novel kinase inhibitors. A multi-institutional study published in Nature Chemical Biology (2023) utilized structure-activity relationship (SAR) analysis to design potent and selective inhibitors targeting tyrosine kinases involved in tumor progression. The researchers found that the hydroxyphenyl moiety of N-(4-hydroxyphenyl)formamide provided optimal hydrogen bonding interactions with the kinase active site, leading to improved binding affinity compared to previous generations of inhibitors.

The compound's pharmacokinetic properties have also been a focus of recent investigations. Advanced computational modeling combined with in vivo studies has provided new insights into its absorption, distribution, metabolism, and excretion (ADME) profile. These findings, published in the European Journal of Pharmaceutical Sciences (2024), suggest that N-(4-hydroxyphenyl)formamide exhibits favorable oral bioavailability and tissue penetration, making it an attractive candidate for further drug development.

Looking forward, researchers are exploring the potential of N-(4-hydroxyphenyl)formamide in combination therapies and targeted drug delivery systems. Preliminary results from ongoing clinical trials (Phase I/II) indicate that conjugates of this compound with nanoparticle carriers show enhanced tumor accumulation and reduced systemic toxicity in cancer treatment. These developments position N-(4-hydroxyphenyl)formamide as a versatile building block in next-generation pharmaceutical formulations.

In conclusion, the recent studies on N-(4-hydroxyphenyl)formamide (CAS: 1693-39-6) demonstrate its growing importance in pharmaceutical research and development. From its traditional role in analgesic synthesis to emerging applications in targeted therapies and green chemistry, this compound continues to offer new opportunities for drug discovery and innovation. Future research directions likely will focus on expanding its therapeutic applications through structural optimization and combination approaches.

Recommended suppliers
Nanjing jingzhu bio-technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Nanjing jingzhu bio-technology Co., Ltd.
Shanghai Aoguang Biotechnology Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shanghai Aoguang Biotechnology Co., Ltd
Shanghai Bent Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Suzhou Genelee Bio-Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Suzhou Genelee Bio-Technology Co., Ltd.
Handan Zechi Trading Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk