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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)-

ethyl 2-(6-bromopyridin-2-yl)acetate

CCOC(=O)Cc1cccc(n1)Br Request for Quotation
Chemical Name: ethyl 2-(6-bromopyridin-2-yl)acetate
CAS Number: 955369-63-8
Product Number: AG00IJ6S(AGN-PC-09RZP5)
Synonyms:
MDL No:
Molecular Formula: C9H10BrNO2
Molecular Weight: 244.0852

Identification/Properties

Computed Properties
Molecular Weight:
244.088g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
242.989g/mol
Monoisotopic Mass:
242.989g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
175
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 2-(6-bromopyridin-2-yl)acetate is a versatile compound commonly used in chemical synthesis for various purposes. It serves as a key building block in the creation of diverse organic molecules due to its unique structural composition and reactivity. In synthetic chemistry, this compound is particularly valued for its ability to participate in multiple types of reactions, such as nucleophilic substitutions, palladium-catalyzed coupling reactions, and esterifications. Its presence in a synthesis scheme can facilitate the construction of more complex molecular structures or the modification of existing ones, offering chemists a powerful tool for designing and producing a wide range of organic compounds with specific properties and functions. Whether employed as a starting material or an intermediate, Ethyl 2-(6-bromopyridin-2-yl)acetate plays a crucial role in the strategic assembly of target molecules in the laboratory, making it a valuable asset for synthetic chemists aiming to generate novel compounds for various applications.