2,3,5,6,8,9-hexahydro-1,4,7,10-Tetraoxacyclododecino[2,3-g]quinolin-15(12H)-one


Chemical Name: 2,3,5,6,8,9-hexahydro-1,4,7,10-Tetraoxacyclododecino[2,3-g]quinolin-15(12H)-one
CAS Number: 1355620-88-0
Product Number: AG009XGH(AGN-PC-0WA5IP)
Synonyms:
MDL No:
Molecular Formula: C15H17NO5
Molecular Weight: 291.2992

Identification/Properties


Computed Properties
Molecular Weight:
291.303g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
291.111g/mol
Monoisotopic Mass:
291.111g/mol
Topological Polar Surface Area:
66A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
386
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:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 2,3,5,6,8,9-Hexahydro-[1,4,7,10]tetraoxacyclododecino[2,3-g]quinolin-15(12H)-one plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable intermediate in the creation of various complex organic molecules. In synthetic chemistry, this compound serves as a key starting material for the construction of heterocyclic frameworks and can be utilized in the synthesis of pharmaceuticals, agrochemicals, and materials. Its cyclic nature and oxygen-containing functional groups enable diverse manipulations such as ring-opening reactions, functional group transformations, and formation of fused ring systems. This compound's presence in a synthesis pathway can lead to the generation of molecular diversity and the production of novel compounds with potential biological activity or material properties.