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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 3-amino-6-bromopyridine-2-carboxylate

CCOC(=O)c1nc(Br)ccc1N Request for Quotation
Chemical Name: ethyl 3-amino-6-bromopyridine-2-carboxylate
CAS Number: 28033-08-1
Product Number: AG003IWX(AGN-PC-04X1MU)
Synonyms:
MDL No:
Molecular Formula: C8H9BrN2O2
Molecular Weight: 245.0733

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
245.076g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
243.985g/mol
Monoisotopic Mass:
243.985g/mol
Topological Polar Surface Area:
65.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
189
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:
Danger
UN#:
2811
Hazard Statements:
H301-H311-H331
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-amino-6-bromopicolinate is a versatile intermediate widely utilized in chemical synthesis processes. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique chemical properties.In chemical synthesis, Ethyl 3-amino-6-bromopicolinate acts as a valuable building block for the construction of diverse molecular structures. Its functional groups enable it to participate in a range of key reactions, including nucleophilic substitution, condensation, and cyclization reactions. This compound serves as a strategic precursor for the introduction of amino and bromine functionalities into target molecules, allowing for the synthesis of complex organic compounds with specific biological or chemical activities.Furthermore, Ethyl 3-amino-6-bromopicolinate offers chemists the flexibility to tailor its structure by incorporating additional functional groups or modifying its substituents. This flexibility in structural modification is essential for designing and optimizing new chemical entities with desired properties for various applications in the fields of medicine, agriculture, and materials science.Overall, Ethyl 3-amino-6-bromopicolinate plays a crucial role in chemical synthesis by serving as a key intermediate that enables the efficient construction of diverse organic molecules with specific properties and functionalities.