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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)-

METHYL 2-CHLORO-5-HYDROXYISONICOTINATE

COC(=O)c1cc(Cl)ncc1O Request for Quotation
Chemical Name: METHYL 2-CHLORO-5-HYDROXYISONICOTINATE
CAS Number: 1256807-90-5
Product Number: AG000ODM(AGN-PC-0WAJ7A)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO3
Molecular Weight: 187.5804

Identification/Properties

Computed Properties
Molecular Weight:
187.579g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
187.004g/mol
Monoisotopic Mass:
187.004g/mol
Topological Polar Surface Area:
59.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-chloro-5-hydroxyisonicotinate is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. In particular, it is commonly employed as a key intermediate in the synthesis of bioactive molecules and pharmaceutical agents due to its functional groups that facilitate further derivatization. Its strategic placement of the chloro and hydroxy groups enables selective transformations, making it valuable for the introduction of specific functional moieties during synthetic procedures. Additionally, the presence of the methyl ester provides handling convenience and enhances its compatibility in various reaction conditions. Overall, Methyl 2-chloro-5-hydroxyisonicotinate plays a pivotal role in the efficient and targeted synthesis of diverse chemical compounds, making it an indispensable tool for organic chemists and researchers alike.