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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 1,2,3,4-tetrahydroquinoline-5-carboxylate

COC(=O)c1cccc2c1CCCN2 Request for Quotation
Chemical Name: methyl 1,2,3,4-tetrahydroquinoline-5-carboxylate
CAS Number: 939758-71-1
Product Number: AG00GSGU(AGN-PC-00VAGD)
Synonyms:
MDL No:
Molecular Formula: C11H13NO2
Molecular Weight: 191.2264

Identification/Properties

Computed Properties
Molecular Weight:
191.23g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
191.095g/mol
Monoisotopic Mass:
191.095g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
217
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 1,2,3,4-tetrahydroquinoline-5-carboxylate is a versatile compound commonly used in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Due to its unique structure and reactivity, this compound plays a crucial role in the development of advanced synthetic methodologies and the formation of complex molecular structures. In particular, it is valued for its ability to participate in a range of chemical reactions, including cycloadditions, reductions, and functional group transformations. Additionally, Methyl 1,2,3,4-tetrahydroquinoline-5-carboxylate is widely employed in the synthesis of heterocyclic compounds, which are essential in drug discovery and materials science. Its significance in chemical synthesis extends to the production of fine chemicals and specialty products with diverse applications in research and industry.