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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)-

(1R)-1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol;hydrobromide

CC1NCCc2c1cc(O)c(c2)O.Br Request for Quotation
Chemical Name: (1R)-1-methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol;hydrobromide
CAS Number: 59709-57-8
Product Number: AG003EGW(AGN-PC-07BYOT)
Synonyms:
MDL No:
Molecular Formula: C10H14BrNO2
Molecular Weight: 260.1277

Identification/Properties

Properties
MP:
186-187°C(lit.);
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
260.131g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
259.021g/mol
Monoisotopic Mass:
259.021g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
186
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydrobromide is a versatile compound that finds widespread application in chemical synthesis due to its unique structural properties and reactivity. This compound serves as a valuable building block in the synthesis of various heterocyclic compounds and pharmaceutical intermediates. In organic synthesis, it acts as a key starting material for the construction of biologically active molecules and complex organic structures. Its hydrobromide form enhances the solubility and stability of the compound, making it easier to handle and manipulate in laboratory settings. By incorporating 1-Methyl-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydrobromide into synthetic routes, chemists can access a diverse range of compounds with potential applications in drug discovery, material science, and medicinal chemistry.