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  2. 2-((5-Chloropyridin-2-yl)amino)2-oxoacetic acid ethyl ester monohydrochloride

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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-((5-Chloropyridin-2-yl)amino)2-oxoacetic acid ethyl ester monohydrochloride

CCOC(=O)C(=O)Nc1ccc(cn1)Cl.Cl Request for Quotation
Chemical Name: 2-((5-Chloropyridin-2-yl)amino)2-oxoacetic acid ethyl ester monohydrochloride
CAS Number: 1243308-37-3
Product Number: AG000LV2(AGN-PC-0WAKBS)
Synonyms:
MDL No:
Molecular Formula: C9H10Cl2N2O3
Molecular Weight: 265.0933

Identification/Properties

Computed Properties
Molecular Weight:
265.09g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
264.007g/mol
Monoisotopic Mass:
264.007g/mol
Topological Polar Surface Area:
68.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
248
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound Ethyl 2-((5-chloropyridin-2-yl)amino)-2-oxoacetate hydrochloride plays a vital role in chemical synthesis as a key intermediate. It serves as a versatile building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique chemical structure, this compound facilitates the introduction of the 5-chloropyridin-2-ylamino group into organic molecules, enabling the synthesis of complex compounds for various applications. Its reactivity and functional groups make it well-suited for forming intricate molecular scaffolds, making it a valuable tool for organic chemists in the design and production of novel compounds.