Cas no 54942-63-1 (2-amino-1-(2-methoxyphenyl)ethan-1-ol)

2-Amino-1-(2-methoxyphenyl)ethan-1-ol is a chiral β-amino alcohol derivative characterized by a methoxy-substituted aromatic ring and a hydroxyl-amine functional group. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structural features, including the presence of both amino and hydroxyl groups, enable its use in asymmetric catalysis and as a building block for bioactive molecules. The methoxy group enhances solubility and influences electronic properties, making it valuable for tailored synthetic applications. High purity and well-defined stereochemistry ensure reproducibility in research and industrial processes. Proper handling and storage under inert conditions are recommended to maintain stability.
2-amino-1-(2-methoxyphenyl)ethan-1-ol structure
54942-63-1 structure
Product Name:2-amino-1-(2-methoxyphenyl)ethan-1-ol
CAS No:54942-63-1
MF:C9H13NO2
MW:167.205022573471
CID:1011694
PubChem ID:3871396
Update Time:2025-06-15

2-amino-1-(2-methoxyphenyl)ethan-1-ol Chemical and Physical Properties

Names and Identifiers

    • BENZENEMETHANOL,α-(AMINOMETHYL)-2-METHOXY-
    • 2-AMINO-1-(2-METHOXYPHENYL)ETHANOL
    • SCHEMBL4582899
    • DB-013376
    • G54394
    • AKOS016051390
    • F2189-0841
    • EN300-39056
    • 54942-63-1
    • 2-amino-1-(2-methoxyphenyl)ethan-1-ol
    • CS-0453498
    • 2-amino-1-(2-methoxyphenyl)ethanol, AldrichCPR
    • CHEMBL4127448
    • AKOS000123094
    • Z336086524
    • BDBM50272926
    • MDL: MFCD03840179
    • Inchi: 1S/C9H13NO2/c1-12-9-5-3-2-4-7(9)8(11)6-10/h2-5,8,11H,6,10H2,1H3
    • InChI Key: ILFKFOKAPPGUOP-UHFFFAOYSA-N
    • SMILES: OC(CN)C1C=CC=CC=1OC

Computed Properties

  • Exact Mass: 167.094628657g/mol
  • Monoisotopic Mass: 167.094628657g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 130
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.1
  • Topological Polar Surface Area: 55.5?2

2-amino-1-(2-methoxyphenyl)ethan-1-ol Security Information

  • Hazard Category Code: 22-36
  • Safety Instruction: 26
  • Hazardous Material Identification: Xn

2-amino-1-(2-methoxyphenyl)ethan-1-ol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
A612553-25mg
2-amino-1-(2-methoxyphenyl)ethan-1-ol
54942-63-1
25mg
$ 50.00 2022-06-08
TRC
A612553-50mg
2-amino-1-(2-methoxyphenyl)ethan-1-ol
54942-63-1
50mg
$ 70.00 2022-06-08
TRC
A612553-250mg
2-amino-1-(2-methoxyphenyl)ethan-1-ol
54942-63-1
250mg
$ 275.00 2022-06-08
A2B Chem LLC
AG36228-50mg
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
50mg
$146.00 2024-04-19
A2B Chem LLC
AG36228-100mg
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
100mg
$200.00 2024-04-19
A2B Chem LLC
AG36228-250mg
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
250mg
$269.00 2024-04-19
A2B Chem LLC
AG36228-500mg
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
500mg
$480.00 2024-04-19
A2B Chem LLC
AG36228-1g
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
1g
$605.00 2024-04-19
A2B Chem LLC
AG36228-2.5g
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
2.5g
$1154.00 2024-04-19
A2B Chem LLC
AG36228-5g
2-Amino-1-(2-methoxyphenyl)ethanol
54942-63-1 95%
5g
$1690.00 2024-04-19

Additional information on 2-amino-1-(2-methoxyphenyl)ethan-1-ol

Recent Advances in the Study of 2-amino-1-(2-methoxyphenyl)ethan-1-ol (CAS: 54942-63-1) and Its Applications in Chemical Biology and Medicine

The compound 2-amino-1-(2-methoxyphenyl)ethan-1-ol (CAS: 54942-63-1) has recently garnered significant attention in the field of chemical biology and medicinal chemistry due to its versatile pharmacological properties and potential therapeutic applications. This research brief aims to provide an overview of the latest findings related to this compound, focusing on its synthesis, biological activities, and emerging applications in drug development.

Recent studies have highlighted the role of 2-amino-1-(2-methoxyphenyl)ethan-1-ol as a key intermediate in the synthesis of various bioactive molecules. Its structural motif, featuring an amino alcohol group and a methoxyphenyl ring, makes it a valuable scaffold for designing novel drugs targeting neurological and cardiovascular diseases. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy as a precursor for developing selective serotonin reuptake inhibitors (SSRIs) with improved pharmacokinetic profiles.

In addition to its synthetic utility, 2-amino-1-(2-methoxyphenyl)ethan-1-ol has shown promising biological activities in preclinical models. Research conducted at leading pharmaceutical institutions has revealed its potential as an anti-inflammatory and neuroprotective agent. Mechanistic studies indicate that the compound modulates key signaling pathways, including the NF-κB and MAPK cascades, which are implicated in chronic inflammatory conditions and neurodegenerative disorders.

Another area of active investigation is the compound's role in cancer therapeutics. A recent publication in Bioorganic & Medicinal Chemistry Letters reported that derivatives of 2-amino-1-(2-methoxyphenyl)ethan-1-ol exhibit potent inhibitory effects on certain cancer cell lines, particularly those associated with breast and prostate cancers. These findings underscore the compound's potential as a lead structure for developing targeted anticancer agents.

From a methodological perspective, advances in analytical techniques have enabled more precise characterization of 2-amino-1-(2-methoxyphenyl)ethan-1-ol and its derivatives. High-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy have been instrumental in elucidating its molecular interactions and stability profiles. Furthermore, computational modeling approaches, such as molecular docking and dynamics simulations, have provided valuable insights into its binding modes with biological targets.

Despite these promising developments, challenges remain in optimizing the compound's bioavailability and reducing potential off-target effects. Ongoing research efforts are focused on structural modifications to enhance its drug-like properties while maintaining its therapeutic efficacy. Collaborative initiatives between academic and industrial researchers are expected to accelerate the translation of these findings into clinical applications.

In conclusion, 2-amino-1-(2-methoxyphenyl)ethan-1-ol (CAS: 54942-63-1) represents a compelling case study in the intersection of chemical biology and drug discovery. Its multifaceted pharmacological profile and synthetic versatility position it as a valuable asset in the development of next-generation therapeutics. Future research directions may include exploring its applications in combination therapies and investigating its mechanisms of action at the molecular level.

Recommended suppliers
Yunnanjiuzhen
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Yunnanjiuzhen
Jiangsu Xinsu New Materials Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jiangsu Xinsu New Materials Co., Ltd
Shenzhen Jianxing Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shenzhen Jianxing Pharmaceutical Technology Co., Ltd.
Nanjing Jubai Biopharm
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Nanjing Jubai Biopharm
Shaanxi pure crystal photoelectric technology co. LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Shaanxi pure crystal photoelectric technology co. LTD