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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)-

2-(6-bromopyridin-2-yl)benzaldehyde

O=Cc1ccccc1c1cccc(n1)Br Request for Quotation
Chemical Name: 2-(6-bromopyridin-2-yl)benzaldehyde
CAS Number: 914349-51-2
Product Number: AG00GRHX(AGN-PC-07A1FU)
Synonyms:
MDL No:
Molecular Formula: C12H8BrNO
Molecular Weight: 262.1020

Identification/Properties

Computed Properties
Molecular Weight:
262.106g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
260.979g/mol
Monoisotopic Mass:
260.979g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
222
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


The 2-(6-Bromopyridin-2-yl)benzaldehyde is a versatile and valuable chemical compound used in various chemical synthesis applications. It serves as a key building block in the creation of organic molecules and serves as an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science research. Its unique structure and reactivity make it a valuable tool in the design and development of new compounds for a wide range of industries. In chemical synthesis, this compound is commonly used as a starting material to introduce specific functional groups or to modify existing molecules, allowing chemists to create complex and diverse chemical structures. Its role in organic synthesis highlights its importance as a fundamental component in the development of new and innovative chemical compounds with potential applications in various fields.