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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-7-hydroxy-, (3S)-

OC(=O)[C@H]1NCc2c(C1)ccc(c2)O Request for Quotation
Chemical Name: 3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-7-hydroxy-, (3S)-
CAS Number: 128502-56-7
Product Number: AG0039OZ(AGN-PC-0O0V43)
Synonyms:
MDL No:
Molecular Formula: C10H11NO3
Molecular Weight: 193.1992

Identification/Properties

Computed Properties
Molecular Weight:
193.202g/mol
XLogP3:
-1.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
193.074g/mol
Monoisotopic Mass:
193.074g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


L-7-Hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly utilized in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure enables it to act as a key intermediate in the production of complex molecules with important biological activities. By incorporating L-7-Hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid into synthetic pathways, chemists are able to access a wide range of functionalized derivatives that exhibit diverse properties and potential applications. Its strategic placement within molecular frameworks allows for efficient and selective transformations, making it an essential component in the toolkit of synthetic chemists seeking to access novel compounds for various industrial purposes.