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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)-

Pyridine, 2-bromo-6-(methylthio)-

CSc1cccc(n1)Br Request for Quotation
Chemical Name: Pyridine, 2-bromo-6-(methylthio)-
CAS Number: 74134-42-2
Product Number: AG005DW6(AGN-PC-0NJENG)
Synonyms:
MDL No:
Molecular Formula: C6H6BrNS
Molecular Weight: 204.0875

Identification/Properties

Properties
BP:
269.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
204.085g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
202.94g/mol
Monoisotopic Mass:
202.94g/mol
Topological Polar Surface Area:
38.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
89.1
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-6-(methylthio)pyridine is a versatile compound used in chemical synthesis for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique structure and functional groups, this compound plays a crucial role in the development of diverse organic compounds. Its application in chemical synthesis includes acting as a key building block in the creation of complex molecules with biological activity. Additionally, 2-Bromo-6-(methylthio)pyridine can be utilized as a reagent in heterocyclic chemistry, allowing for the formation of novel structures with potential applications in drug discovery and materials science. Its ability to undergo various reactions and transformations makes it a valuable tool for synthetic chemists looking to access new chemical entities with promising properties.