528099
8-Amino-6-methoxyquinoline hydrobromide
97%
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About This Item
Empirical Formula (Hill Notation):
C10H10N2O · HBr
CAS Number:
Molecular Weight:
255.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C10H10N2O.BrH/c1-13-8-5-7-3-2-4-12-10(7)9(11)6-8;/h2-6H,11H2,1H3;1H
SMILES string
Br.COc1cc(N)c2ncccc2c1
InChI key
WGYQQCWLZRGIKB-UHFFFAOYSA-N
assay
97%
mp
238 °C (dec.) (lit.)
General description
8-Amino-6-methoxyquinoline hydrobromide is a quinoline building block. It is formed during the synthesis of α-morpholino-β-(N-8-amino-6-methoxyquinoline)-benzylacetophenone.
Application
8-Amino-6-methoxyquinoline hydrobromide may be used as an amino component in a novel series of bladder-selective diaminocyclobutenedione potassium channel openers. It may also be used for the synthesis of 1-N-(6-methoxy-8-quinoyl)-4′-carboxyl-benzensulfonamide.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Armer RE, et al.
Bioorganic & Medicinal Chemistry, 9, 2430-2430 (1999)
Butera JA.
Journal of Medicinal Chemistry, 43, 1187-1187 (2000)
Iris Boll et al.
Bioorganic & medicinal chemistry letters, 16(10), 2781-2785 (2006-02-24)
Two ligand-intercalator-peptide nucleic acid conjugates (L-NADI-PNAs) have been synthesized. Affinity of these conjugates to their complementary DNAs was found to be affected by Zn(2+). The magnitude of this effect could be controlled by a variation of the ligand. Upon binding
a, ?-Diamino Ketones. III. 1 Reaction of 8-Amino-6-methoxyquinoline with a-Bromo-?-aminoketones.
Cromwell NH and Hoeksema H.
Journal of the American Chemical Society, 67(1), 124-125 (1945)
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