Compound Identification
SMILES
CN1C(=O)C2=C(SC3=C2CC(C)(C)OC3)N2CCCN=C12
InChIKey
InChIKey=PHQKJPYAGNXPLK-UHFFFAOYSA-N
Formula
C15H19N3O2S
Mass
305.4
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
- Class Thienopyrans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Thienopyrans
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Thienopyrans
Alternative Parents
3,4,5-trisubstituted-2-aminothiophenes Pyrans Hydropyrimidines Vinylogous amides Heteroaromatic compounds Guanidines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Dialkyl ethers Carboxylic acids and derivatives Carboximidamides Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thienopyran - 3,4,5-trisubstituted-2-aminothiophene - Hydropyrimidine - 1,4,5,6-tetrahydropyrimidine - Pyran - 2-aminothiophene - Heteroaromatic compound - Thiophene - Vinylogous amide - Guanidine - Carboxylic acid derivative - Dialkyl ether - Ether - Oxacycle - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as thienopyrans. These are heterocyclic compounds containing a thiophene ring fused to a pyran ring. Thiophene is 5-membered ring consisting of four carbon atoms and one sulfur atom. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.
External Descriptors
Not available