N-methyl-1-(5-methylthiophen-2-yl)methanamine;hydrochloride


Chemical Name: N-methyl-1-(5-methylthiophen-2-yl)methanamine;hydrochloride
CAS Number: 912569-78-9
Product Number: AG00GVNU(AGN-PC-01EK6M)
Synonyms:
MDL No:
Molecular Formula: C7H12ClNS
Molecular Weight: 177.6949

Identification/Properties


Computed Properties
Molecular Weight:
177.69g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
177.038g/mol
Monoisotopic Mass:
177.038g/mol
Topological Polar Surface Area:
40.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
85
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-Thiophenemethanamine, N,5-dimethyl-, hydrochloride (1:1) is a versatile compound commonly used in chemical synthesis for its unique properties and reactivity. In synthesis, this compound serves as a key building block in the formation of various organic molecules, owing to its ability to undergo a variety of reactions.One of the primary applications of 2-Thiophenemethanamine, N,5-dimethyl-, hydrochloride (1:1) in chemical synthesis is in the production of heterocyclic compounds. By reacting this compound with suitable reagents, chemists can form complex heterocycles such as thiazoles, benzothiazoles, and other sulfur-containing rings. These heterocycles are widely used in pharmaceuticals, agrochemicals, and materials science.Additionally, this compound plays a crucial role in the synthesis of various biologically active molecules. Chemists can modify the structure of 2-Thiophenemethanamine, N,5-dimethyl-, hydrochloride (1:1) to introduce specific functional groups or substituents, thus creating potential drug candidates or molecular probes for biological studies.Furthermore, in material science, the reactivity of 2-Thiophenemethanamine, N,5-dimethyl-, hydrochloride (1:1) can be harnessed to generate novel polymers and organic frameworks with unique properties. By incorporating this compound into polymerization reactions or supramolecular assemblies, researchers can design materials with tailored functionalities for various applications.Overall, 2-Thiophenemethanamine, N,5-dimethyl-, hydrochloride (1:1) is a valuable tool in chemical synthesis, enabling the creation of diverse molecules with applications across pharmaceuticals, materials science, and beyond.