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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-Cyano-2-(hydroxyimino)acetic acid ethyl ester, potassium salt

[O-]/N=C(/C(=O)OCC)C#N.[K+] Request for Quotation
Chemical Name: 2-Cyano-2-(hydroxyimino)acetic acid ethyl ester, potassium salt
CAS Number: 158014-03-0
Product Number: AG00HYGY(AGN-PC-0WBOJB)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
180.204g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
179.994g/mol
Monoisotopic Mass:
179.994g/mol
Topological Polar Surface Area:
85.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
205
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Cyano-2-(hydroxyimino)acetic acid ethyl ester, potassium salt is a versatile compound widely used in chemical synthesis, particularly in the field of organic chemistry. With its unique chemical structure, this compound serves as a valuable reagent in various reactions due to its ability to act as both a nucleophile and an electrophile.In organic synthesis, this compound is commonly employed in the formation of heterocycles, which are essential building blocks in pharmaceutical and agrochemical industries. Its ability to participate in diverse reaction mechanisms makes it a valuable tool for the creation of complex molecular structures with precision and efficiency.Furthermore, the potassium salt form of 2-Cyano-2-(hydroxyimino)acetic acid ethyl ester offers improved solubility and stability compared to other forms, making it easier to handle and manipulate in laboratory settings. Its compatibility with a wide range of reaction conditions and substrates further enhances its utility in chemical synthesis, allowing for the streamlined production of various organic compounds.Overall, the application of 2-Cyano-2-(hydroxyimino)acetic acid ethyl ester, potassium salt in chemical synthesis showcases its importance as a key component in the toolkit of synthetic chemists, enabling the efficient and precise construction of complex molecules for diverse applications.