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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, 2,5-dichloro-

Clc1ccc2c(c1)nc(s2)Cl Request for Quotation
Chemical Name: Benzothiazole, 2,5-dichloro-
CAS Number: 2941-48-2
Product Number: AG0035YY(AGN-PC-00M0MW)
Synonyms:
MDL No:
Molecular Formula: C7H3Cl2NS
Molecular Weight: 204.0764

Identification/Properties

Properties
MP:
64-66°C
BP:
286.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;Keep in dry area;Keep container tightly closed;
Form:
Solid
Computed Properties
Molecular Weight:
204.068g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
202.936g/mol
Monoisotopic Mass:
202.936g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dichlorobenzothiazole is a potent chemical compound commonly used in chemical synthesis processes. Its versatile nature allows for numerous applications in various industries, particularly in the production of rubber and plastics. This compound serves as a critical intermediate in the synthesis of accelerators used in rubber vulcanization, where it promotes the cross-linking of rubber molecules to enhance its strength and durability. Additionally, 2,5-Dichlorobenzothiazole plays a key role in the creation of pharmaceuticals, agrochemicals, and dyes. Its unique structure and reactivity make it an indispensable tool for chemists seeking to develop novel materials and compounds with enhanced properties.