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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)-

5-methyl-1,2,3,4-tetrahydroquinoline;hydrochloride

Cc1cccc2c1CCCN2.Cl Request for Quotation
Chemical Name: 5-methyl-1,2,3,4-tetrahydroquinoline;hydrochloride
CAS Number: 861368-85-6
Product Number: AG008FDR(AGN-PC-09T3VY)
Synonyms:
MDL No:
Molecular Formula: C10H14ClN
Molecular Weight: 183.6779

Identification/Properties

Computed Properties
Molecular Weight:
183.679g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
183.081g/mol
Monoisotopic Mass:
183.081g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
133
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methyl-1,2,3,4-tetrahydroquinoline hydrochloride is a key intermediate in chemical synthesis due to its versatile applications. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a crucial component in the synthesis of complex organic molecules.One notable application of 5-Methyl-1,2,3,4-tetrahydroquinoline hydrochloride is in the development of novel drug molecules. By incorporating this compound into drug synthesis processes, chemists can access a diverse range of pharmacologically active compounds with potential therapeutic benefits. Additionally, its presence in medicinal chemistry laboratories facilitates the creation of new drug candidates with improved efficacy and reduced side effects.Furthermore, this compound plays a significant role in the synthesis of specialty chemicals and materials. Its use in chemical reactions enables the construction of intricate molecular frameworks, making it indispensable for the creation of advanced materials with tailored properties. Chemists leverage the unique characteristics of 5-Methyl-1,2,3,4-tetrahydroquinoline hydrochloride to design and produce innovative products across various industries.Overall, the application of 5-Methyl-1,2,3,4-tetrahydroquinoline hydrochloride in chemical synthesis underscores its importance as a versatile and indispensable compound for creating a wide array of organic molecules with diverse functionalities.