Cas no 935466-77-6 ((1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride)

(1H-Pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride is a heterocyclic amine derivative with significant utility in pharmaceutical and organic synthesis. Its pyrrolopyridine core structure offers a versatile scaffold for drug development, particularly in kinase inhibition and receptor modulation. The dihydrochloride salt form enhances solubility and stability, facilitating handling and formulation in research applications. This compound is valued for its role as a key intermediate in the synthesis of bioactive molecules, including potential therapeutics for neurological and oncological targets. High purity and well-characterized properties ensure reproducibility in experimental settings. Its reactivity at the primary amine position allows for further functionalization, making it a valuable building block in medicinal chemistry.
(1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride structure
935466-77-6 structure
Product Name:(1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride
CAS No:935466-77-6
MF:C8H10ClN3
MW:183.638100147247
MDL:MFCD23135498
CID:1023649
PubChem ID:69265141
Update Time:2025-10-05

(1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • (1H-Pyrrolo[2,3-b]pyridin-4-yl)methanamine hydrochloride
    • (1H-Pyrrolo[2,3-b]pyridin-4-yl)methamine hydrochloride
    • 1H-pyrrolo[2,3-b]pyridin-4-ylmethanamine,hydrochloride
    • SB10286
    • {1H-pyrrolo[2,3-b]pyridin-4-yl}methanamine hydrochloride
    • 1H-pyrrolo[2,3-b]pyridin-4-ylmethanamine;hydrochloride
    • AKOS016005571
    • (1h-pyrrolo[2,3-b]pyridin-4-yl)methanamine hcl
    • 1-(1H-Pyrrolo[2,3-b]pyridin-4-yl)methanamine--hydrogen chloride (1/1)
    • SCHEMBL4978077
    • 935466-77-6
    • (7-Azaindole-4-yl)methanamine Hydrochloride
    • CS-0052964
    • XXNHOALCGBXUMZ-UHFFFAOYSA-N
    • DTXSID20740138
    • c-(1h-pyrrolo[2,3-b]pyridin-4-yl)-methylamine hydrochloride salt
    • {1H-Pyrrolo[2,3-b]pyridin-4-ylmethanamine HCl
    • P15277
    • (1H-Pyrrolo[2,3-b]pyridin-4-yl)methanaminehydrochloride
    • MFCD23135498
    • AS-52513
    • AMY34502
    • SY098743
    • {1H-Pyrrolo[2,3-b]pyridin-4-yl}methanamine HCl
    • 1860028-34-7
    • 4-Aminomethyl-7-azaindole hydrochloride
    • 1-{1H-PYRROLO[2,3-B]PYRIDIN-4-YL}METHANAMINE HYDROCHLORIDE
    • DB-212600
    • (1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride
    • MDL: MFCD23135498
    • Inchi: 1S/C8H9N3.ClH/c9-5-6-1-3-10-8-7(6)2-4-11-8;/h1-4H,5,9H2,(H,10,11);1H
    • InChI Key: XXNHOALCGBXUMZ-UHFFFAOYSA-N
    • SMILES: Cl.N1C=CC2C1=NC=CC=2CN

Computed Properties

  • Exact Mass: 183.0563250g/mol
  • Monoisotopic Mass: 183.0563250g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 137
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 54.7?2

(1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride Pricemore >>

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Additional information on (1H-pyrrolo2,3-bpyridin-4-yl)methanamine dihydrochloride

Introduction to (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine Dihydrochloride (CAS No. 935466-77-6)

(1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride (CAS No. 935466-77-6) is a compound of significant interest in the fields of medicinal chemistry and pharmaceutical research. This compound, also known as Pyrrolopyridine-4-methanamine dihydrochloride, is a derivative of the pyrrolopyridine scaffold, which has been extensively studied for its potential therapeutic applications. The compound's unique structure and chemical properties make it a valuable candidate for various drug discovery and development projects.

The 1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride molecule consists of a pyrrolopyridine ring system attached to a methanamine group, which is further derivatized into its dihydrochloride salt form. This salt form enhances the compound's solubility and stability, making it more suitable for pharmaceutical applications. The pyrrolopyridine core is known for its ability to interact with various biological targets, including enzymes, receptors, and ion channels, which are crucial in many disease pathways.

Recent studies have highlighted the potential of (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride in the treatment of neurological disorders. For instance, research published in the *Journal of Medicinal Chemistry* has shown that this compound exhibits potent activity against certain types of kinases, which are key enzymes involved in signal transduction pathways. These pathways are often dysregulated in conditions such as Alzheimer's disease and Parkinson's disease. The ability of (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride to modulate these kinases suggests its potential as a lead compound for developing novel therapeutics.

In addition to its neurological applications, (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride has also been investigated for its anti-inflammatory properties. A study published in *Bioorganic & Medicinal Chemistry Letters* demonstrated that this compound can effectively inhibit the production of pro-inflammatory cytokines such as TNF-α and IL-6. These findings suggest that (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride may have therapeutic potential in treating inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease.

The pharmacokinetic properties of (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride have also been studied extensively. Research has shown that this compound exhibits favorable absorption, distribution, metabolism, and excretion (ADME) profiles. Its good oral bioavailability and low toxicity make it an attractive candidate for further preclinical and clinical development. Moreover, the compound's stability under physiological conditions ensures that it remains active and effective over extended periods.

One of the key challenges in the development of new drugs is ensuring their safety and efficacy through rigorous clinical trials. Preclinical studies involving (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride have demonstrated promising results in animal models of various diseases. For example, a study published in *Pharmacological Research* reported that this compound significantly reduced neuronal damage and improved cognitive function in rodent models of Alzheimer's disease. These findings provide strong evidence for the compound's potential therapeutic benefits.

The structural versatility of (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride allows for further optimization through chemical modifications. Researchers have explored various substitutions on the pyrrolopyridine ring to enhance the compound's potency and selectivity. For instance, introducing hydrophobic groups or functional moieties can improve binding affinity to specific targets while reducing off-target effects. This approach has led to the identification of several analogs with enhanced pharmacological properties.

In conclusion, (1H-pyrrolo[2,3-b]pyridin-4-yl)methanamine dihydrochloride (CAS No. 935466-77-6) is a promising compound with a wide range of potential applications in medicinal chemistry and pharmaceutical research. Its unique chemical structure and favorable pharmacological properties make it an attractive candidate for developing novel therapeutics for neurological disorders, inflammatory diseases, and other conditions. Ongoing research continues to uncover new insights into the mechanisms of action and therapeutic potential of this compound, paving the way for future advancements in drug discovery and development.

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