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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-chloro-2-(chloromethyl)-4-methylquinoline;hydrochloride

ClCc1nc2ccccc2c(c1Cl)C.Cl Request for Quotation
Chemical Name: 3-chloro-2-(chloromethyl)-4-methylquinoline;hydrochloride
CAS Number: 37781-33-2
Product Number: AG00CLO9(AGN-PC-00VC5G)
Synonyms:
MDL No:
Molecular Formula: C11H10Cl3N
Molecular Weight: 262.5628

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
262.558g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
260.988g/mol
Monoisotopic Mass:
260.988g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
198
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

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Chemical Structure


3-Chloro-2-(chloromethyl)-4-methylquinoline hydrochloride is a versatile compound widely used in chemical synthesis. One key application of this compound is as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the introduction of specific functional groups and modifications, making it a valuable intermediate in the production of complex molecules. Additionally, 3-Chloro-2-(chloromethyl)-4-methylquinoline hydrochloride is used as a reagent in the preparation of heterocyclic compounds with potential biological activity. Its role in chemical synthesis extends to the creation of novel materials and compounds with diverse applications in research and industry.