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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)-

6,7-dimethoxy-3,4-dihydroisoquinoline;hydrochloride

COc1cc2C=NCCc2cc1OC.Cl Request for Quotation
Chemical Name: 6,7-dimethoxy-3,4-dihydroisoquinoline;hydrochloride
CAS Number: 20232-39-7
Product Number: AG002864(AGN-PC-0KK0DR)
Synonyms:
MDL No: MFCD00143492
Molecular Formula: C11H14ClNO2
Molecular Weight: 227.6874

Identification/Properties

Properties
MP:
198-202 °C
BP:
322.9 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
227.688g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
227.071g/mol
Monoisotopic Mass:
227.071g/mol
Topological Polar Surface Area:
30.8A^2
Heavy Atom Count:
15
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302+H312+H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-Dimethoxy-3,4-Dihydroisoquinoline Hydrochloride is a versatile compound widely utilized in chemical synthesis as a key intermediate in the production of various pharmaceuticals and organic compounds. Its unique structure and reactivity make it an essential building block for the synthesis of complex molecules with diverse applications.In chemical synthesis, this compound serves as a crucial component in the creation of novel drugs, research chemicals, and specialty compounds. Its specific chemical properties allow it to participate in various reactions, such as condensation, alkylation, and oxidation, enabling the formation of intricate molecular structures with specific pharmacological or industrial properties.Additionally, 6,7-Dimethoxy-3,4-Dihydroisoquinoline Hydrochloride can be employed in the development of new methodologies for organic synthesis, providing chemists with a valuable tool for exploring innovative pathways to desired products. Its presence in synthesis routes contributes to the efficiency, selectivity, and overall success of chemical processes, making it a valuable asset in the realm of synthetic chemistry.