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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-(chloromethyl)-4-(3-methoxypropoxy)-3-methylpyridine;hydrochloride

Cc1c(OCCCOC)ccnc1CCl.Cl Request for Quotation
Chemical Name: 2-(chloromethyl)-4-(3-methoxypropoxy)-3-methylpyridine;hydrochloride
CAS Number: 153259-31-5
Product Number: AG003H2M(AGN-PC-022KT4)
Synonyms:
MDL No: MFCD06658231
Molecular Formula: C11H17Cl2NO2
Molecular Weight: 266.1642

Identification/Properties

Properties
MP:
113-115°C
BP:
360 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
266.162g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
265.064g/mol
Monoisotopic Mass:
265.064g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
169
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-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


2-(Chloromethyl)-4-(3-methoxypropoxy)-3-methylpyridine hydrochloride is a versatile compound widely used in chemical synthesis as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential building block in the creation of various organic compounds.In chemical synthesis, this compound acts as a valuable starting material for the synthesis of heterocyclic compounds, which are essential in the development of new drug candidates. Its chloromethyl group allows for selective functionalization reactions, enabling the introduction of different functional groups to tailor the properties of the final compound.Furthermore, the presence of the methoxypropoxy group offers opportunities for the incorporation of additional substituents, allowing for further diversification of the molecular structure. This versatility makes 2-(Chloromethyl)-4-(3-methoxypropoxy)-3-methylpyridine hydrochloride a valuable tool in the hands of synthetic chemists looking to design and synthesize novel compounds with specific biological activities or chemical properties.