1. Home
  2. methyl 6-(chloromethyl)pyridine-3-carboxylate hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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 6-(chloromethyl)pyridine-3-carboxylate hydrochloride

COC(=O)c1ccc(nc1)CCl.Cl Request for Quotation
Chemical Name: methyl 6-(chloromethyl)pyridine-3-carboxylate hydrochloride
CAS Number: 951306-53-9
Product Number: AG019RFZ(AGN-PC-0WO4ZE)
Synonyms:
MDL No: MFCD16036539
Molecular Formula: C8H9Cl2NO2
Molecular Weight: 222.0686

Identification/Properties

Computed Properties
Molecular Weight:
222.065g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
221.001g/mol
Monoisotopic Mass:
221.001g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
163
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Methyl 6-(chloromethyl)nicotinate hydrochloride is a versatile compound with valuable applications in chemical synthesis. This compound serves as an important building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure, it can be selectively modified to introduce specific functional groups, making it a valuable intermediate in the synthesis of complex molecules. Its chloromethyl group is particularly useful for facilitating reactions such as nucleophilic substitutions and palladium-catalyzed cross-coupling reactions. By incorporating Methyl 6-(chloromethyl)nicotinate hydrochloride into synthetic pathways, chemists can access a wide range of structurally diverse compounds with potential applications in drug discovery and material science.