Cas no 1211497-01-6 (C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride)

C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride is a heterocyclic amine derivative featuring a thiazole core with a methyl substituent at the 2-position. The hydrochloride salt form enhances its stability and solubility, making it suitable for synthetic applications in pharmaceutical and agrochemical research. The thiazole moiety is a key structural motif in bioactive compounds, contributing to its utility as an intermediate in the synthesis of potential drug candidates. Its well-defined chemical properties and high purity ensure consistent performance in coupling reactions and derivatization processes. This compound is particularly valuable for medicinal chemistry applications, where precise structural modifications are required for target molecule development.
C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride structure
1211497-01-6 structure
Product Name:C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride
CAS No:1211497-01-6
MF:C5H9ClN2S
MW:164.656358480453
MDL:MFCD03419480
CID:1082352
PubChem ID:24206439
Update Time:2025-05-20

C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Methyl-4-thiazolemethanamine hydrochloride
    • (2-methyl-1,3-thiazol-4-yl)methanamine,hydrochloride
    • C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride
    • (2-methyl-1,3-thiazol-4-yl)methanamine;hydrochloride
    • (2-Methyl-thiazol-4-yl)methylamine hydrochloride
    • MFCD03419480
    • SY332623
    • D86402
    • (2-methyl-1,3-thiazol-4-yl)methanamine hydrochloride
    • SCHEMBL7017198
    • (2-Methylthiazol-4-yl)methanamine hydrochloride
    • SB31750
    • WS-02090
    • 1-(2-METHYL-1,3-THIAZOL-4-YL)METHANAMINE HYDROCHLORIDE
    • (2-methylthiazol-4-yl)methanamine;hydrochloride
    • 1211497-01-6
    • (2-Methylthiazol-4-yl)methanaminehydrochloride
    • (2-Methyl-4-thiazolyl)methanamine Hydrochloride
    • CS-0309751
    • MDL: MFCD03419480
    • Inchi: 1S/C5H8N2S.ClH/c1-4-7-5(2-6)3-8-4;/h3H,2,6H2,1H3;1H
    • InChI Key: MMBJJIGTSNIQJZ-UHFFFAOYSA-N
    • SMILES: Cl.S1C=C(CN)N=C1C

Computed Properties

  • Exact Mass: 164.0174972g/mol
  • Monoisotopic Mass: 164.0174972g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 76.8
  • 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: 67.2?2

C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride Security Information

C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride Pricemore >>

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C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride Related Literature

Additional information on C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride

C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride: A Comprehensive Overview

C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride, also known by its CAS number 1211497-01-6, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound has garnered attention due to its unique chemical structure and potential applications in drug development. The molecule consists of a thiazole ring, a methyl group, and an amine functional group, which collectively contribute to its diverse chemical properties.

The thiazole ring, a key structural component of this compound, is a five-membered aromatic heterocycle containing one sulfur and one nitrogen atom. This ring system is known for its stability and ability to participate in various chemical reactions. The methyl group attached to the thiazole ring at the 4-position further enhances the compound's reactivity and selectivity. The amine group, on the other hand, introduces basicity and can act as a nucleophile in certain reactions.

Recent studies have explored the synthesis of C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride through various routes. One common method involves the reaction of 2-methylthiazole with an appropriate alkylating agent in the presence of a base. The hydrochloride salt is typically formed by protonation of the amine group under acidic conditions. Researchers have also investigated the stereochemistry and regioselectivity of these reactions to optimize yield and purity.

In terms of applications, C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride has shown promise in medicinal chemistry. Its ability to act as a precursor for more complex molecules makes it valuable in drug design. For instance, derivatives of this compound have been studied for their potential as inhibitors of certain enzymes or receptors, which could lead to novel therapeutic agents.

Moreover, the compound's stability under various conditions has been extensively studied. Research indicates that C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride is stable at room temperature and exhibits minimal degradation under normal storage conditions. However, exposure to strong oxidizing agents or extreme pH levels can lead to decomposition.

From an environmental perspective, the biodegradability and toxicity of C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride have been assessed in recent studies. These findings suggest that the compound has low toxicity to aquatic organisms and can be safely disposed of through standard waste management practices.

In conclusion, C-(2-Methyl-thiazol-4-yl)-methylamine hydrochloride (CAS 1211497-01-6) is a versatile compound with a wide range of potential applications in organic synthesis and pharmacology. Its unique chemical structure and favorable properties make it an attractive target for further research and development.

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