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64973-79-1 | Isoquinoline, dihydro-
CAS No: 64973-79-1 Catalog No: AG00H77Y MDL No:
Product Description
Catalog Number:
AG00H77Y
Chemical Name:
Isoquinoline, dihydro-
CAS Number:
64973-79-1
Molecular Formula:
C9H9N
Molecular Weight:
131.1745
IUPAC Name:
1,2-dihydroisoquinoline
InChI:
InChI=1S/C9H9N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-6,10H,7H2
InChI Key:
IOEPOEDBBPRAEI-UHFFFAOYSA-N
SMILES:
C1=Cc2c(CN1)cccc2
Properties
Complexity:
140
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
131.073g/mol
Formal Charge:
0
Heavy Atom Count:
10
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
131.178g/mol
Monoisotopic Mass:
131.073g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
12A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2
Literature
| Title | Journal |
|---|---|
| Solution-phase parallel synthesis of a diverse library of 1,2-dihydroisoquinolines. | ACS combinatorial science 20110509 |
| Uncovering the structure of human red hair pheomelanin: benzothiazolylthiazinodihydroisoquinolines as key building blocks. | Journal of natural products 20110425 |
| Silver triflate and N-heterocyclic carbene co-catalyzed reaction of N'-(2-alkynylbenzylidene)hydrazide, methanol with alpha,beta-unsaturated aldehyde. | Chemical communications (Cambridge, England) 20100914 |
| Gold(I)-catalyzed tandem reactions initiated by hydroamination of alkynyl carbamates: application to the synthesis of nitidine. | The Journal of organic chemistry 20091204 |
| AgOTf-catalyzed tandem reaction of N'-(2-alkynylbenzylidene)hydrazide with alkyne. | Chemical communications (Cambridge, England) 20090621 |
| 1,2-dihydroisoquinolines as templates for cascade reactions to access isoquinoline alkaloid frameworks. | Organic letters 20071122 |
| Lewis acid- and organocatalyst-cocatalyzed multicomponent reactions of 2-alkynylbenzaldehydes, amines, and ketones. | Organic letters 20071122 |
| Synthesis of functionalized 1,2-dihydroisoquinolines via multicomponent one-pot reaction of 2-alkynylbenzaldehyde, amine, zinc, and allylic bromide or benzyl bromide. | The Journal of organic chemistry 20071026 |
| Concise synthesis of 1,2-dihydroisoquinolines and 1H-isochromenes by carbophilic lewis acid-catalyzed tandem nucleophilic addition and cyclization of 2-(1-alkynyl)arylaldimines and 2-(1-alkynyl)arylaldehydes. | The Journal of organic chemistry 20070608 |
| Pd(II)-catalyzed asymmetric addition of malonates to dihydroisoquinolines. | Journal of the American Chemical Society 20061101 |
| 3D pharmacophore models for 1,2,3,4-tetrahydroisoquinoline derivatives acting as anticonvulsant agents. | Archiv der Pharmazie 20060701 |
| In(OTf)3-catalyzed tandem nucleophilic addition and cyclization of ortho-alkynylarylaldimines to 1,2-dihydroisoquinolines. | Angewandte Chemie (International ed. in English) 20060602 |
| Organocatalytic diastereo- and enantioselective annulation reactions--construction of optically active 1,2-dihydroisoquinoline and 1,2-dihydrophthalazine derivatives. | Angewandte Chemie (International ed. in English) 20050919 |
| Synthetic strategy toward skeletal diversity via solid-supported, otherwise unstable reactive intermediates. | Angewandte Chemie (International ed. in English) 20040319 |
| In vitro and in vivo evaluations of dihydroquinoline- and dihydroisoquinoline-based targetor moieties for brain-specific chemical delivery systems. | Journal of drug targeting 20020201 |
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