[1,3]Benzodioxolo[5,6-c]phenanthridinium, 1,2-dimethoxy-12-methyl-,chloride


Chemical Name: [1,3]Benzodioxolo[5,6-c]phenanthridinium, 1,2-dimethoxy-12-methyl-,chloride
CAS Number: 3895-92-9
Product Number: AG0032KU(AGN-PC-0RI6IC)
Synonyms:
MDL No:
Molecular Formula: C21H18ClNO4
Molecular Weight: 383.8249

Identification/Properties


Properties
MP:
195-205 °C
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
383.828g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
383.092g/mol
Monoisotopic Mass:
383.092g/mol
Topological Polar Surface Area:
40.8A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
516
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#:
-
Hazard Statements:
H302+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1,2-dimethoxy-12-methyl[1,3]benzodioxolo[5,6-c]phenanthridinium chloride is a versatile compound that finds wide application in chemical synthesis processes. This unique molecule serves as an important intermediate in the synthesis of various organic compounds due to its distinct chemical properties.In chemical synthesis, 1,2-dimethoxy-12-methyl[1,3]benzodioxolo[5,6-c]phenanthridinium chloride acts as a key reagent for the formation of heterocyclic structures and aromatic compounds. It is commonly used as a catalyst or reactant in the production of pharmaceuticals, agrochemicals, and other fine chemicals.The presence of the benzodioxole and phenanthridinium moieties in the molecule imparts specific reactivity, allowing for selective functionalization and diversification in multistep synthesis routes. This compound enables chemists to access complex molecular scaffolds efficiently, thereby facilitating the development of novel compounds with potential biological activities.Overall, the use of 1,2-dimethoxy-12-methyl[1,3]benzodioxolo[5,6-c]phenanthridinium chloride in chemical synthesis plays a crucial role in the advancement of organic chemistry research and the discovery of new chemical entities with diverse applications.