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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Benzothiazolamine, 5,7-dimethyl-

Cc1cc(C)c2c(c1)nc(s2)N Request for Quotation
Chemical Name: 2-Benzothiazolamine, 5,7-dimethyl-
CAS Number: 73351-87-8
Product Number: AG00FE0R(AGN-PC-0KBJMX)
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5,7-Dimethylbenzo[d]thiazol-2-amine is a versatile compound widely utilized in chemical synthesis as a key building block for the creation of various organic molecules. This specific amine derivative serves as a valuable intermediate in the development of pharmaceuticals, agrochemicals, and specialty chemicals due to its unique molecular structure and reactivity. In chemical synthesis, 5,7-Dimethylbenzo[d]thiazol-2-amine acts as a crucial component in the formation of complex organic compounds through various reactions such as nucleophilic substitution, reductive amination, and cross-coupling processes. With its diverse applications in synthetic chemistry, this compound plays a pivotal role in the creation of innovative materials and functionalized molecules tailored for specific industrial and research purposes.