Compound Identification
SMILES
OC[C@@]1(OC2=CC=CC=C2[N+]([O-])=O)OC[C@@H](O)[C@@H](O)[C@@H]1O
InChIKey
InChIKey=CMROAFQUZBOIMS-YJQGPUDQSA-N
Formula
C12H15NO8
Mass
301.251
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic oxygen compounds
-
Class
Organooxygen compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Level 5
Glycosyl compounds
- Level 6 Phenolic glycosides
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Level 5
Glycosyl compounds
-
Subclass
Carbohydrates and carbohydrate conjugates
-
Class
Organooxygen compounds
-
Superclass
Organic oxygen compounds
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Glycosyl compounds
Direct Parent
Phenolic glycosides
Alternative Parents
Nitrobenzenes Nitroaromatic compounds Phenol ethers Phenoxy compounds Ketals Monosaccharides Oxanes Secondary alcohols Oxacyclic compounds Organic oxoazanium compounds Polyols Propargyl-type 1,3-dipolar organic compounds Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenolic glycoside - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Ketal - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - C-nitro compound - Organic nitro compound - Secondary alcohol - Acetal - Organic oxoazanium - Oxacycle - Organoheterocyclic compound - Polyol - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Primary alcohol - Organic salt - Organic zwitterion - Organic oxide - Hydrocarbon derivative - Alcohol - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
External Descriptors
Not available