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522-57-6

522-57-6 | (6,7-dimethoxy-1-isoquinolyl) (3,4-dimethoxyphenyl) ketone

CAS No: 522-57-6 Catalog No: AG00DAO2 MDL No:

Product Description

Catalog Number:
AG00DAO2
Chemical Name:
(6,7-dimethoxy-1-isoquinolyl) (3,4-dimethoxyphenyl) ketone
CAS Number:
522-57-6
IUPAC Name:
(6,7-dimethoxyisoquinolin-1-yl)-(3,4-dimethoxyphenyl)methanone
InChI:
InChI=1S/C20H19NO5/c1-23-15-6-5-13(10-16(15)24-2)20(22)19-14-11-18(26-4)17(25-3)9-12(14)7-8-21-19/h5-11H,1-4H3
InChI Key:
QJTBIAMBPGGIGI-UHFFFAOYSA-N
EC Number:
208-331-4
UNII:
L8825LX0F5
NSC Number:
94266

Properties

Complexity:
473  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
353.126g/mol
Formal Charge:
0
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
353.374g/mol
Monoisotopic Mass:
353.126g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
66.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.7  

Literature

Title Journal
Synthesis, cytotoxic and antimalarial activities of benzoyl thiosemicarbazone analogs of isoquinoline and related compounds. Molecules (Basel, Switzerland) 20100223
Kinetics of photooxidation of papaverine hydrochloride and its major photooxidation products. Journal of pharmaceutical and biomedical analysis 20060616
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Isoquinoline derivatives as potential acetylcholinesterase inhibitors. Bioorganic & medicinal chemistry letters 20060415
Oxidation and degradation products of papaverine. Part II[1]: investigations on the photochemical degradation of papaverine solutions. Archiv der Pharmazie 20030901
Photooxidation of papaverine, papaverinol and papaveraldine in their chloroform solutions. Acta poloniae pharmaceutica 20020101

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