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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, 5-chloro-

Clc1ccc2c(c1)ncs2 Request for Quotation
Chemical Name: Benzothiazole, 5-chloro-
CAS Number: 2786-51-8
Product Number: AG002UYS(AGN-PC-0019B7)
Synonyms:
MDL No:
Molecular Formula: C7H4ClNS
Molecular Weight: 169.6314

Identification/Properties

Properties
MP:
105 - 107℃
BP:
267.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
169.626g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
168.975g/mol
Monoisotopic Mass:
168.975g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
131
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Chlorobenzothiazole, a versatile compound widely used in chemical synthesis, serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. With its unique chemical structure, 5-Chlorobenzothiazole plays a crucial role in the development of innovative therapeutic agents and the modification of existing drugs. Its application in organic chemistry extends to the synthesis of heterocyclic compounds, offering opportunities for the investigation and development of new reaction pathways. Additionally, 5-Chlorobenzothiazole's reactivity and functional groups make it a valuable precursor in the production of specialty chemicals and advanced materials, contributing to the advancement of diverse industries.