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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)-

3-Pyridinecarboxylic acid, 6-(bromomethyl)-, ethyl ester

CCOC(=O)c1ccc(nc1)CBr Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-(bromomethyl)-, ethyl ester
CAS Number: 178264-57-8
Product Number: AG0025VP(AGN-PC-03MUTD)
Synonyms:
MDL No:
Molecular Formula: C9H10BrNO2
Molecular Weight: 244.0852

Identification/Properties

Computed Properties
Molecular Weight:
244.088g/mol
XLogP3:
1.7
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#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 6-(bromomethyl)nicotinate is a versatile chemical compound commonly employed in various chemical synthesis applications. Due to its unique structure, this compound serves as a key building block in the construction of complex organic molecules. In organic synthesis, it is frequently used as a bromine-containing reagent for introducing functional groups into target molecules through substitution reactions. This compound's bromomethyl group adds a valuable dimension to its reactivity, allowing chemists to modify and functionalize organic molecules with precision. Additionally, Ethyl 6-(bromomethyl)nicotinate plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials science due to its ability to facilitate the synthesis of diverse molecular structures with specific properties and functions. Its application in chemical synthesis showcases its significance as a valuable tool for creating novel compounds with tailored properties in various fields of research and industry.