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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)-

5-bromo-1,3-benzothiazole-2-carbaldehyde

O=Cc1nc2c(s1)ccc(c2)Br Request for Quotation
Chemical Name: 5-bromo-1,3-benzothiazole-2-carbaldehyde
CAS Number: 885279-64-1
Product Number: AG004598(AGN-PC-07CNC2)
Synonyms:
MDL No:
Molecular Formula: C8H4BrNOS
Molecular Weight: 242.0925

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
242.09g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
240.92g/mol
Monoisotopic Mass:
240.92g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
190
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-Bromobenzothiazole-2-carbaldehyde is a versatile chemical compound commonly used in chemical synthesis processes. Its application in organic synthesis is particularly notable due to its unique properties and reactivity.1. Precursor for pharmaceuticals: 5-Bromobenzothiazole-2-carbaldehyde serves as a key building block in the synthesis of various pharmaceutical compounds. It can be utilized in the production of potential drug candidates, enabling the development of new medications with enhanced therapeutic properties.2. Functional group manipulation: This compound's specific chemical structure allows for efficient manipulation of functional groups during synthetic processes. It can be employed to introduce specific functionalities or modify existing groups in target molecules, facilitating the creation of structurally diverse compounds.3. Catalyst in organic reactions: 5-Bromobenzothiazole-2-carbaldehyde can act as a catalyst in several organic transformations, promoting the formation of complex molecular structures with high efficiency. Its catalytic properties make it a valuable tool for selective reactions and the synthesis of intricate organic molecules.4. Intermediate in synthesis pathways: As an essential intermediate in various synthesis pathways, this compound plays a vital role in linking different chemical reactions. It enables the stepwise assembly of complex molecules by providing a crucial connection between precursor molecules and final products.5. Research tool in organic chemistry: Researchers often utilize 5-Bromobenzothiazole-2-carbaldehyde as a research tool to explore new synthetic strategies and investigate novel chemical reactions. Its versatile nature and reactivity make it a valuable resource for advancing the field of organic chemistry.In summary, 5-Bromobenzothiazole-2-carbaldehyde's significance in chemical synthesis lies in its diverse applications, ranging from pharmaceutical development to catalysis and research. Its role as a versatile building block and functional group modifier makes it an indispensable component in the toolbox of synthetic chemists.