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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)-

Benzothiazole, 2,6-dimethyl-

Cc1ccc2c(c1)sc(n2)C Request for Quotation
Chemical Name: Benzothiazole, 2,6-dimethyl-
CAS Number: 2941-71-1
Product Number: AG003G5K(AGN-PC-0JLPWD)
Synonyms:
MDL No:
Molecular Formula: C9H9NS
Molecular Weight: 163.2395

Identification/Properties

Properties
BP:
132°C/20mmHg(lit.)
Storage:
Keep in dry area;2-8℃;
Refractive Index:
1.6050-1.6090
Computed Properties
Molecular Weight:
163.238g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
163.046g/mol
Monoisotopic Mass:
163.046g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,6-Dimethylbenzo[d]thiazole, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis. Thanks to its unique molecular structure, this compound is a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2,6-Dimethylbenzo[d]thiazole serves as a crucial intermediate in the formation of complex organic molecules. Its incorporation into different chemical reactions leads to the generation of novel compounds with diverse properties and functionalities. This compound's presence can alter the reactivity and selectivity of reactions, allowing for the development of specific molecular structures essential in the production of high-value chemicals.Moreover, the introduction of 2,6-Dimethylbenzo[d]thiazole in chemical synthesis enables researchers to explore new pathways for the design and synthesis of advanced materials. By manipulating the molecular properties of this compound, scientists can tailor the characteristics of the resulting materials, such as electronic properties, optical properties, and molecular recognition capabilities.Overall, the strategic use of 2,6-Dimethylbenzo[d]thiazole in chemical synthesis plays a crucial role in expanding the scope of organic chemistry and facilitating the creation of innovative compounds with diverse applications across various industries.