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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, 4,7-dichloro-

Nc1nc2c(s1)c(Cl)ccc2Cl Request for Quotation
Chemical Name: 2-Benzothiazolamine, 4,7-dichloro-
CAS Number: 1849-70-3
Product Number: AG00ADQY(AGN-PC-0KBJMT)
Synonyms:
MDL No:
Molecular Formula: C7H4Cl2N2S
Molecular Weight: 219.0911

Identification/Properties

Computed Properties
Molecular Weight:
219.083g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
217.947g/mol
Monoisotopic Mass:
217.947g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
181
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


4,7-Dichlorobenzo[d]thiazol-2-amine is a versatile compound commonly used in chemical synthesis as a key building block for the creation of various organic compounds. With its unique structure and reactive properties, this molecule serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 4,7-Dichlorobenzo[d]thiazol-2-amine can be employed as a starting material for the generation of complex molecules through a series of well-established reactions such as coupling reactions, nucleophilic substitutions, and condensations. Its halogenated benzothiazole backbone offers multiple points of reactivity, allowing for the introduction of different functional groups and structural modifications to tailor the properties of the final products.Due to its strategic position within the molecular framework, 4,7-Dichlorobenzo[d]thiazol-2-amine plays a crucial role in diversifying chemical structures and enhancing the biological activities of synthesized compounds. Its presence in the synthetic route can impact the overall efficiency, selectivity, and yield of the desired products, making it an indispensable component in the toolbox of organic chemists and drug discovery researchers.