| Record Information |
|---|
| Version | 1.0 |
|---|
| Created at | 2020-04-27 16:31:52 UTC |
|---|
| Updated at | 2021-01-04 20:37:46 UTC |
|---|
| CannabisDB ID | CDB005551 |
|---|
| Secondary Accession Numbers | Not Available |
|---|
| Cannabis Compound Identification |
|---|
| Common Name | 2-Methyl-1,5-naphthyridine |
|---|
| Description | 2-Methyl-1,5-naphthyridine, also known as 2-methy-1,5-diazanaphthalene, belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton has two fused pyridine rings, with unshared nitrogens at positions 1 and 5. 2-Methyl-1,5-naphthyridine is a strongly basic compound. 2-Methyl-1,5-naphthyridine is a methylated derivative of 1,5-naphthyridine. 2-Methyl-1,5-naphthyridine is one of several structural isomers of ethyl-1,5-naphthyridine which is substituted by a methyl group at different positions. Methyl-1,5-naphthyridines are found in marijuana smoke ( Ref:DOI ). 2-Methyl-1,5-naphthyridine is formed during the combustion of cannabis. |
|---|
| Structure | |
|---|
| Synonyms | | Value | Source |
|---|
| Goldinomycin | MeSH | | N Methylkirromycin | MeSH | | N-Methylkirromycin | MeSH | | Goldinodox | MeSH | | Aurodox | MeSH | | Antibiotic X 5108 | MeSH |
|
|---|
| Chemical Formula | C9H8N2 |
|---|
| Average Molecular Weight | 144.18 |
|---|
| Monoisotopic Molecular Weight | 144.0687 |
|---|
| IUPAC Name | 2-methyl-1,5-naphthyridine |
|---|
| Traditional Name | 2-methyl-1,5-naphthyridine |
|---|
| CAS Registry Number | 7675-32-3 |
|---|
| SMILES | CC1=NC2=C(C=C1)N=CC=C2 |
|---|
| InChI Identifier | InChI=1S/C9H8N2/c1-7-4-5-8-9(11-7)3-2-6-10-8/h2-6H,1H3 |
|---|
| InChI Key | KIWHWEDXEGNASX-UHFFFAOYSA-N |
|---|
| Chemical Taxonomy |
|---|
| Description | Belongs to the class of organic compounds known as naphthyridines. Naphthyridines are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom. |
|---|
| Kingdom | Organic compounds |
|---|
| Super Class | Organoheterocyclic compounds |
|---|
| Class | Diazanaphthalenes |
|---|
| Sub Class | Naphthyridines |
|---|
| Direct Parent | Naphthyridines |
|---|
| Alternative Parents | |
|---|
| Substituents | - Naphthyridine
- Methylpyridine
- Pyridine
- Heteroaromatic compound
- Azacycle
- Organic nitrogen compound
- Organopnictogen compound
- Hydrocarbon derivative
- Organonitrogen compound
- Aromatic heteropolycyclic compound
|
|---|
| Molecular Framework | Aromatic heteropolycyclic compounds |
|---|
| External Descriptors | Not Available |
|---|
| Ontology |
|---|
|
Not Available | | Physical Properties |
|---|
| State | Not Available |
|---|
| Experimental Properties | | Property | Value | Reference |
|---|
| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | logP | Not Available | Not Available |
|
|---|
| Predicted Properties | [] |
|---|
