7-Methyl-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride


Chemical Name: 7-Methyl-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride
CAS Number: 1810069-89-6
Product Number: AG0022KK(AGN-PC-0WAM9W)
Synonyms:
MDL No:
Molecular Formula: C11H16ClN
Molecular Weight: 197.7044

Identification/Properties


Computed Properties
Molecular Weight:
197.706g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
197.097g/mol
Monoisotopic Mass:
197.097g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
155
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



7-Methyl-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This molecule plays a crucial role in various reactions and processes within the field of organic chemistry. Specifically, it serves as a key intermediate for the synthesis of complex organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, $name$ is often employed as a starting material for the preparation of more elaborate molecules due to its unique structural properties and reactivity. Its specific structure allows for functional group manipulations and regioselective transformations, making it a valuable building block in the creation of diverse organic structures. By incorporating $name$ into synthetic pathways, chemists can access a wide range of potential products with tailored properties and functionalities. Furthermore, the presence of the amine group in the structure of 7-Methyl-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride facilitates various types of chemical reactions, such as reductive amination, nucleophilic substitutions, and condensation reactions. This enables chemists to introduce nitrogen-containing moieties into target molecules and enhance the biological or chemical activity of the final products. Overall, the strategic utilization of $name$ in chemical synthesis offers a pathway to efficiently access complex and valuable compounds for both academic and industrial applications.