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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, 1,6-dihydro-6-oxo-, ethyl ester

CCOC(=O)c1ccc(=O)[nH]c1 Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 1,6-dihydro-6-oxo-, ethyl ester
CAS Number: 18617-50-0
Product Number: AG007SFV(AGN-PC-0JPEVK)
Synonyms:
MDL No:
Molecular Formula: C8H9NO3
Molecular Weight: 167.1620

Identification/Properties

Computed Properties
Molecular Weight:
167.164g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
167.058g/mol
Monoisotopic Mass:
167.058g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
266
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-hydroxynicotinate is a versatile compound that finds wide application in chemical synthesis. As a key building block in organic chemistry, this compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, Ethyl 6-hydroxynicotinate is utilized for its ability to introduce the hydroxyl and nicotinate functionalities into complex molecules. Its presence in the synthesis process enables chemists to access a diverse range of products with enhanced biological activities and chemical properties. In pharmaceutical research, Ethyl 6-hydroxynicotinate is often employed for the preparation of potential drug candidates targeting various diseases. Its presence in the molecular structure of these compounds can enhance their solubility, stability, and bioavailability, thereby improving their overall efficacy. Furthermore, in agrochemical development, Ethyl 6-hydroxynicotinate plays a crucial role in the design and synthesis of novel pesticides and herbicides. By incorporating this compound into the molecular framework of agrochemicals, researchers can create compounds with improved environmental profiles and targeted modes of action. Overall, Ethyl 6-hydroxynicotinate's significance in chemical synthesis lies in its ability to facilitate the creation of complex molecules with tailored properties, positioning it as a valuable tool for advancing research and innovation in various fields of chemistry.