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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-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-, ethyl ester,hydrochloride, (S)-

CCOC(=O)[C@H]1NCc2c(C1)cccc2.Cl Request for Quotation
Chemical Name: 3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-, ethyl ester,hydrochloride, (S)-
CAS Number: 15912-56-8
Product Number: AG001QI1(AGN-PC-0Q7MEL)
Synonyms:
MDL No:
Molecular Formula: C12H16ClNO2
Molecular Weight: 241.7139

Identification/Properties

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


H-Tic-Oet·HCl is a versatile compound commonly used in chemical synthesis as a key reagent. In organic chemistry, it serves a crucial role in the formation of various organic compounds through its unique properties and reactions. When employed in synthetic pathways, H-Tic-Oet·HCl can act as a catalyst or a precursor in the creation of complex molecules. Its specific chemical structure allows for selective transformations and functional group modifications, making it a valuable tool for chemists and researchers in the field. Furthermore, H-Tic-Oet·HCl has found applications in medicinal chemistry, where its controlled reactivity can be utilized to design and synthesize pharmaceuticals with enhanced biological activity. Overall, the significance of H-Tic-Oet·HCl in chemical synthesis lies in its ability to enable the efficient and strategic construction of diverse organic molecules with desired properties.