2,1,3-benzothiadiazol-4-ylmethanamine;hydrochloride


Chemical Name: 2,1,3-benzothiadiazol-4-ylmethanamine;hydrochloride
CAS Number: 830330-21-7
Product Number: AG00535A(AGN-PC-0KL7DB)
Synonyms:
MDL No:
Molecular Formula: C7H8ClN3S
Molecular Weight: 201.6765

Identification/Properties


Properties
MP:
223-227℃
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
201.672g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
201.013g/mol
Monoisotopic Mass:
201.013g/mol
Topological Polar Surface Area:
80A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
142
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



Benzo[c][1,2,5]thiadiazol-4-ylmethanamine hydrochloride is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a key building block in the preparation of various organic compounds. Due to its unique structure and reactivity, this compound can undergo a variety of chemical transformations, making it a valuable tool in the creation of novel molecules with diverse properties.In chemical synthesis, Benzo[c][1,2,5]thiadiazol-4-ylmethanamine hydrochloride serves as a precursor for the synthesis of biologically active compounds, pharmaceuticals, agrochemicals, and materials with specialized functions. By incorporating this compound into synthetic pathways, chemists can access a wide range of functional groups and molecular structures, enabling the development of new drugs, polymers, and other advanced materials.Furthermore, the presence of the thiadiazole ring in Benzo[c][1,2,5]thiadiazol-4-ylmethanamine hydrochloride imparts unique electronic and structural properties to the resulting molecules, making them highly sought after in various fields of research and industry. Overall, the compound's versatility and reactivity make it an indispensable reagent in the realm of chemical synthesis, driving innovation and discovery in the molecular sciences.