Cas no 436088-87-8 (5-Amino-1-cyclopentyl-1H-pyrazol-3-ol)

5-Amino-1-cyclopentyl-1H-pyrazol-3-ol is a heterocyclic compound featuring a pyrazole core substituted with an amino group at the 5-position and a hydroxyl group at the 3-position, along with a cyclopentyl moiety at the 1-position. This structure imparts versatility in synthetic applications, particularly as a building block in medicinal chemistry and agrochemical research. The presence of both amino and hydroxyl functional groups enhances its reactivity, enabling derivatization for the development of biologically active molecules. Its cyclopentyl substituent contributes to steric and electronic modulation, influencing binding affinity in target interactions. The compound is valued for its potential in constructing pharmacophores and intermediates for drug discovery.
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol structure
436088-87-8 structure
Product Name:5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
CAS No:436088-87-8
MF:C8H13N3O
MW:167.208321332932
MDL:MFCD02241043
CID:333216
PubChem ID:801265
Update Time:2025-06-08

5-Amino-1-cyclopentyl-1H-pyrazol-3-ol Chemical and Physical Properties

Names and Identifiers

    • 3H-Pyrazol-3-one,5-amino-1-cyclopentyl-1,2-dihydro-
    • 5-AMINO-1-CYCLOPENTYL-1 H -PYRAZOL-3-OL
    • 3-amino-2-cyclopentyl-1H-pyrazol-5-one
    • Oprea1_441156
    • WS-01521
    • MLS000716853
    • AKOS000591024
    • FT-0676665
    • Oprea1_361160
    • CHEMBL1411968
    • 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol, AldrichCPR
    • Oprea1_787794
    • D86529
    • HMS2658D15
    • 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
    • CS-0327317
    • BAS 02913153
    • DTXSID40355440
    • SMR000278370
    • 436088-87-8
    • STK841121
    • MDL: MFCD02241043
    • Inchi: 1S/C8H13N3O/c9-7-5-8(12)10-11(7)6-3-1-2-4-6/h5-6H,1-4,9H2,(H,10,12)
    • InChI Key: PLEUJIDJQYIEKB-UHFFFAOYSA-N
    • SMILES: O=C1C=C(N)N(C2CCCC2)N1

Computed Properties

  • Exact Mass: 167.10600
  • Monoisotopic Mass: 167.106
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 231
  • 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: 0.7
  • Topological Polar Surface Area: 58.4?2

Experimental Properties

  • Density: 1.252
  • Boiling Point: 391.3°C at 760 mmHg
  • Flash Point: 190.4°C
  • Refractive Index: 1.591
  • PSA: 64.07000
  • LogP: 1.86720

5-Amino-1-cyclopentyl-1H-pyrazol-3-ol Security Information

  • Hazard Category Code: 25
  • Safety Instruction: 45
  • Hazardous Material Identification: Xi
  • HazardClass:IRRITANT

5-Amino-1-cyclopentyl-1H-pyrazol-3-ol Customs Data

  • HS CODE:2933199090
  • Customs Data:

    China Customs Code:

    2933199090

    Overview:

    2933199090. Other structurally non fused pyrazole ring compounds. 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:

    2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

5-Amino-1-cyclopentyl-1H-pyrazol-3-ol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A049005869-1g
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8 95%
1g
$941.60 2023-09-01
TRC
A636758-10mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
10mg
$ 50.00 2022-06-07
TRC
A636758-50mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
50mg
$ 135.00 2022-06-07
TRC
A636758-100mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
100mg
$ 210.00 2022-06-07
eNovation Chemicals LLC
Y1048846-50mg
5-AMINO-1-CYCLOPENTYL-1H-PYRAZOL-3-OL
436088-87-8 95%
50mg
$305 2024-06-06
eNovation Chemicals LLC
Y1048846-250mg
5-AMINO-1-CYCLOPENTYL-1H-PYRAZOL-3-OL
436088-87-8 95%
250mg
$845 2024-06-06
A2B Chem LLC
AG18384-1mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
1mg
$73.00 2023-12-30
A2B Chem LLC
AG18384-2mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
2mg
$86.00 2023-12-30
A2B Chem LLC
AG18384-3mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
3mg
$105.00 2023-12-30
A2B Chem LLC
AG18384-5mg
5-Amino-1-cyclopentyl-1H-pyrazol-3-ol
436088-87-8
5mg
$118.00 2023-12-30

Additional information on 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol

Research Brief on 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol (CAS: 436088-87-8): Recent Advances and Applications

The compound 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol (CAS: 436088-87-8) has garnered significant attention in the field of chemical biology and medicinal chemistry due to its unique structural properties and potential therapeutic applications. Recent studies have explored its role as a key intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and antimicrobial agents. This research brief aims to summarize the latest findings related to this compound, highlighting its synthetic pathways, biological activities, and potential clinical relevance.

One of the most notable advancements in the study of 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol is its application in the design of selective kinase inhibitors. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent inhibitory activity against cyclin-dependent kinases (CDKs), which are critical targets in cancer therapy. The researchers utilized a structure-activity relationship (SAR) approach to optimize the compound's binding affinity, resulting in derivatives with improved selectivity and reduced off-target effects. These findings underscore the potential of 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol as a scaffold for developing next-generation anticancer agents.

In addition to its role in kinase inhibition, recent research has also explored the antimicrobial properties of 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol. A study published in Bioorganic & Medicinal Chemistry Letters (2024) reported that this compound and its analogs exhibit broad-spectrum activity against drug-resistant bacterial strains, including methicillin-resistant Staphylococcus aureus (MRSA). The mechanism of action appears to involve disruption of bacterial cell wall synthesis, making it a promising candidate for addressing the growing challenge of antibiotic resistance. Further preclinical studies are underway to evaluate its pharmacokinetic and safety profiles.

The synthetic accessibility of 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol has also been a focus of recent investigations. A novel, high-yield synthesis route was reported in Organic Process Research & Development (2023), which employs a one-pot cyclization strategy under mild conditions. This method not only improves the scalability of the compound but also reduces the environmental impact associated with traditional synthetic approaches. Such advancements are critical for facilitating the large-scale production of this compound for both research and potential clinical applications.

Looking ahead, the versatility of 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol continues to inspire new research directions. Ongoing studies are exploring its utility in other therapeutic areas, such as neurodegenerative diseases and inflammatory disorders. Moreover, computational modeling and artificial intelligence-driven drug design are being leveraged to further optimize its pharmacological properties. As the body of evidence grows, this compound is poised to play an increasingly important role in the development of novel therapeutics.

In conclusion, 5-Amino-1-cyclopentyl-1H-pyrazol-3-ol (CAS: 436088-87-8) represents a promising scaffold in medicinal chemistry, with demonstrated applications in oncology, antimicrobial therapy, and beyond. The recent advancements in its synthesis, biological evaluation, and mechanistic understanding highlight its potential to address unmet medical needs. Future research should focus on translating these findings into clinical applications, while also exploring new derivatives with enhanced efficacy and safety profiles.

Recommended suppliers
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Amadis Chemical Company Limited
SHOCHEM(SHANGHAI) CO.,lTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
SHOCHEM(SHANGHAI) CO.,lTD
Hubei Cuiyuan Biotechnology Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hubei Cuiyuan Biotechnology Co.,Ltd
Shenzhen Yaoyuan R&D Center Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shenzhen Yaoyuan R&D Center Co.,Ltd