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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)-

6-bromo-4-methylpyridine-3-carbaldehyde

Cc1cc(Br)ncc1C=O Request for Quotation
Chemical Name: 6-bromo-4-methylpyridine-3-carbaldehyde
CAS Number: 926294-07-7
Product Number: AG006FR0(AGN-PC-0CLS11)
Synonyms:
MDL No:
Molecular Formula: C7H6BrNO
Molecular Weight: 200.0326

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
200.035g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
198.963g/mol
Monoisotopic Mass:
198.963g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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:
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


6-Bromo-4-methylnicotinaldehyde, a versatile chemical compound, is frequently employed in organic synthesis for its unique properties and reactivity. Its use in chemical reactions often leads to the formation of novel structures and compounds that are crucial for various industries and research fields.One of the primary applications of 6-Bromo-4-methylnicotinaldehyde in chemical synthesis is as a key intermediate in the production of pharmaceuticals. This compound serves as a building block in the synthesis of various active pharmaceutical ingredients (APIs) due to its ability to undergo selective transformations to introduce specific functional groups and stereochemistry required for drug efficacy.Furthermore, 6-Bromo-4-methylnicotinaldehyde is utilized in the preparation of heterocyclic compounds, which are fundamental in medicinal chemistry and material science. Its reactivity towards different nucleophiles and electrophiles enables the construction of complex molecular frameworks, essential for the development of new materials with advanced properties.In addition, this compound is also employed in the synthesis of agrochemicals, dyes, and flavoring agents, showcasing its diverse applicability across multiple industries. Overall, the strategic incorporation of 6-Bromo-4-methylnicotinaldehyde in chemical synthesis plays a crucial role in expanding the repertoire of available compounds, driving innovation, and advancing scientific research.