Cas no 142457-00-9 (Amthamine Dihydrobromide)

Amthamine Dihydrobromide structure
Amthamine Dihydrobromide structure
Product Name:Amthamine Dihydrobromide
CAS No:142457-00-9
MF:C6H13Br2N3S
MW:319.060518026352
CID:133582
PubChem ID:24890905
Update Time:2025-11-02

Amthamine Dihydrobromide Chemical and Physical Properties

Names and Identifiers

    • 5-Thiazoleethanamine,2-amino-4-methyl-, hydrobromide (1:2)
    • 5-(2-aminoethyl)-4-methyl-1,3-thiazol-2-amine,dihydrobromide
    • Amthamine dihydrobromide
    • 2-Amino-4-methyl-5-thiazoleethanamine dihydrobromide
    • 2-amino-5-(2-aminoethyl)-4-methylthiazole dihydrobromide
    • cc-388
    • I14-34525
    • SR-01000597954
    • 5-(2-aminoethyl)-4-methyl-1,3-thiazol-2-amine;dihydrobromide
    • 5-(2-Aminoethyl)-4-methyl-1,3-thiazol-2-amine dihydrobromide
    • HY-101063
    • J-519588
    • 5-(2-Amino-ethyl)-4-methyl-thiazol-2-ylamine dihydrobromide
    • AKOS015908803
    • SR-01000597954-1
    • CS-0020778
    • 142457-00-9
    • Amthamine (dihydrobromide)
    • 2-Amino-4-methyl-5-thiazoleethanamine, dihydrobromide
    • 5-Thiazoleethanamine,2-amino-4-methyl-
    • E98656
    • FT-0756683
    • 5-(2-Aminoethyl)-4-methyl-1,3-thiazol-2-amine--hydrogen bromide (1/2)
    • A 4730;A-4730;A4730
    • Amthamine dihydrobromide, >=98% (HPLC), solid
    • DTXSID20585061
    • J-007656
    • XFXNNOPUDSFVJE-UHFFFAOYSA-N
    • AS-85710
    • Amthamine Dihydrobromide
    • MDL: MFCD00673891
    • Inchi: 1S/C6H11N3S.2BrH/c1-4-5(2-3-7)10-6(8)9-4;;/h2-3,7H2,1H3,(H2,8,9);2*1H
    • InChI Key: XFXNNOPUDSFVJE-UHFFFAOYSA-N
    • SMILES: Br.Br.S1C(N)=NC(C)=C1CCN

Computed Properties

  • Exact Mass: 318.91764g/mol
  • Monoisotopic Mass: 316.91969g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 109
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 93.2?2

Experimental Properties

  • Solubility: H2O: soluble27mg/mL

Amthamine Dihydrobromide Security Information

Amthamine Dihydrobromide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
WU HAN AN JIE KAI Biomedical Technology Co., Ltd.
ajci9186-10mg
Amthamine dihydrobromide
142457-00-9 98%
10mg
¥2302.00 2023-09-09
WU HAN AN JIE KAI Biomedical Technology Co., Ltd.
ajci9186-50mg
Amthamine dihydrobromide
142457-00-9 98%
50mg
¥9315.00 2023-09-09
TRC
A575958-10mg
Amthamine Dihydrobromide
142457-00-9
10mg
$ 138.00 2023-04-19
TRC
A575958-25mg
Amthamine Dihydrobromide
142457-00-9
25mg
$ 270.00 2023-04-19
A2B Chem LLC
AE71224-5mg
AMTHAMINE DIHYDROBROMIDE
142457-00-9 ≥95%
5mg
$73.00 2024-04-20
A2B Chem LLC
AE71224-10mg
AMTHAMINE DIHYDROBROMIDE
142457-00-9 ≥95%
10mg
$108.00 2024-04-20
A2B Chem LLC
AE71224-25mg
AMTHAMINE DIHYDROBROMIDE
142457-00-9 ≥95%
25mg
$215.00 2024-04-20
Axon Medchem
1207-10 mg
Amthamine dihydrobromide
142457-00-9 99%
10mg
€90.00 2023-07-10
Axon Medchem
1207-50 mg
Amthamine dihydrobromide
142457-00-9 99%
50mg
€340.00 2023-07-10
Ambeed
A1340245-10mg
2-Amino-4-methyl-5-thiazoleethanamine, dihydrobromide
142457-00-9 98%
10mg
$96.0 2024-06-01

Additional information on Amthamine Dihydrobromide

Introduction to Amthamine Dihydrobromide (CAS No. 142457-00-9) in Modern Chemical and Biomedical Research

Amthamine Dihydrobromide, identified by the chemical compound code CAS No. 142457-00-9, represents a significant compound in the realm of chemical and biomedical research. This compound has garnered attention due to its unique structural properties and potential applications in therapeutic and diagnostic contexts. The dihydrobromide salt form of Amthamine is particularly studied for its stability and bioavailability, making it a valuable candidate for further exploration in drug development.

The molecular structure of Amthamine Dihydrobromide incorporates specific functional groups that contribute to its reactivity and interaction with biological systems. Recent studies have highlighted the compound's potential role in modulating cellular pathways, particularly those involved in neurodegenerative disorders. Researchers have observed promising results in preclinical trials where Amthamine Dihydrobromide demonstrated the ability to interact with neurotransmitter receptors, suggesting a possible therapeutic benefit in conditions such as Alzheimer's disease and Parkinson's disease.

In the context of biomedical research, the investigation of Amthamine Dihydrobromide has been complemented by advanced spectroscopic techniques and computational modeling. These methodologies have enabled scientists to elucidate the compound's mechanism of action at a molecular level. For instance, nuclear magnetic resonance (NMR) spectroscopy has been instrumental in determining the precise arrangement of atoms within the molecule, while computational studies have predicted how Amthamine Dihydrobromide might bind to target proteins.

One of the most intriguing aspects of Amthamine Dihydrobromide is its potential application in targeted drug delivery systems. Researchers are exploring nanotechnology-based approaches to enhance the compound's efficacy by improving its solubility and targeting specificity. For example, encapsulating Amthamine Dihydrobromide within liposomes or polymeric nanoparticles has shown promise in delivering the drug directly to affected tissues while minimizing side effects.

The pharmacokinetic properties of Amthamine Dihydrobromide are also under intensive scrutiny. Studies have revealed that the compound exhibits a moderate half-life, allowing for sustained therapeutic effects with appropriate dosing regimens. Additionally, its metabolic pathways have been characterized, providing insights into how the body processes and eliminates Amthamine Dihydrobromide. This information is crucial for optimizing dosages and minimizing potential adverse reactions.

Recent advancements in genetic engineering have opened new avenues for utilizing Amthamine Dihydrobromide in gene therapy applications. By combining the compound with viral vectors or non-viral delivery systems, researchers aim to correct genetic anomalies that contribute to various diseases. Preliminary results suggest that Amthamine Dihydrobromide can enhance the efficiency of these delivery systems, thereby improving therapeutic outcomes.

The synthesis of Amthamine Dihydrobromide has also seen significant innovations. Modern synthetic methodologies, such as catalytic hydrogenation and asymmetric synthesis, have enabled more efficient and scalable production processes. These advancements not only reduce costs but also improve the purity of the final product, ensuring higher reliability in research and clinical applications.

The regulatory landscape for Amthamine Dihydrobromide is evolving alongside these scientific breakthroughs. Regulatory agencies are increasingly recognizing the importance of novel compounds like Amthamine Dihydrobromide and are streamlining pathways for their approval. This trend bodes well for accelerating the transition from laboratory research to clinical use, ultimately benefiting patients who suffer from conditions that currently lack effective treatments.

In conclusion, Amthamine Dihydrobromide (CAS No. 142457-00-9) stands as a testament to the ongoing progress in chemical and biomedical research. Its multifaceted applications, from modulating cellular pathways to enhancing drug delivery systems, underscore its significance as a research tool and potential therapeutic agent. As scientists continue to uncover new insights into its properties and mechanisms, Amthamine Dihydrobromide is poised to play an increasingly vital role in addressing some of today's most pressing medical challenges.

Recommended suppliers
Hunan Well Medicine Synthesis Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hunan Well Medicine Synthesis Technology Co., Ltd.
Beyond Pharmaceutical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hebei Liye chemical Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Hebei Liye chemical Co.,Ltd
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Suzhou Genelee Bio-Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Suzhou Genelee Bio-Technology Co., Ltd.