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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-5-chloropyridine-2-carboxylate

CCOC(=O)c1ncc(cc1N)Cl Request for Quotation
Chemical Name: ethyl 3-amino-5-chloropyridine-2-carboxylate
CAS Number: 27330-35-4
Product Number: AG00BHQA(AGN-PC-0JPAYW)
Synonyms:
MDL No:
Molecular Formula: C8H9ClN2O2
Molecular Weight: 200.6223

Identification/Properties

Properties
BP:
345.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-amino-5-chloropicolinate is a versatile compound that finds wide applicability in chemical synthesis processes. This unique compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, Ethyl 3-amino-5-chloropicolinate acts as a key intermediate for the preparation of diverse heterocyclic compounds, which are essential in drug development and material science. Its structural features make it a valuable starting material in the synthesis of complex molecules with biological activities. Additionally, Ethyl 3-amino-5-chloropicolinate exhibits reactivity that enables it to participate in numerous functionalization reactions, thereby expanding its synthetic utility in the production of novel chemical entities.