4,7-dimethyl-1,3-benzothiazol-2-amine


Chemical Name: 4,7-dimethyl-1,3-benzothiazol-2-amine
CAS Number: 78584-08-4
Product Number: AG008MGZ(AGN-PC-0KBJMW)
Synonyms:
MDL No:
Molecular Formula: C9H10N2S
Molecular Weight: 178.2541

Identification/Properties


Computed Properties
Molecular Weight:
178.253g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
178.056g/mol
Monoisotopic Mass:
178.056g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
174
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:
1
Compound Is Canonicalized:
Yes

Safety Information


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

NMR Spectrum


Other Analytical Data


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Chemical Structure



4,7-Dimethylbenzo[d]thiazol-2-amine, also known as $name$, is a versatile compound widely used in chemical synthesis for various applications. In particular, this compound is commonly utilized as a building block in the development of pharmaceuticals, agrochemicals, and materials science.One of the key applications of 4,7-Dimethylbenzo[d]thiazol-2-amine in chemical synthesis is as a key intermediate in the preparation of bioactive compounds and drug molecules. Its unique chemical structure and reactivity make it a valuable starting material for creating new compounds with potential therapeutic properties.Furthermore, 4,7-Dimethylbenzo[d]thiazol-2-amine is often employed in the synthesis of fluorescent dyes and probes used in biological imaging and diagnostics. Its ability to undergo various chemical transformations allows for the introduction of specific functional groups that can modify the properties of the final product, making it an essential tool in the field of chemical biology.Additionally, this compound is an important building block in the production of specialty chemicals and materials due to its structural diversity and compatibility with different synthetic methodologies. Its presence in the synthesis of polymers, catalysts, and other advanced materials highlights its significance in modern chemical research and development.