| Record Information |
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| Version | 1.0 |
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| Created at | 2020-07-28 20:27:13 UTC |
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| Updated at | 2020-11-18 16:40:18 UTC |
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| CannabisDB ID | CDB006320 |
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| Secondary Accession Numbers | Not Available |
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| Cannabis Compound Identification |
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| Common Name | Spiroteramat |
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| Description | Spirotetramat, also known as movento, belongs to the class of organic compounds known as p-xylenes. These are aromatic compounds that contain a p-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 4-positions. This enol is more stable due to double bond being in a ring and the conjugation with the amide group and the benzene ring. It is ambimobile, being transported both upwards and downwards through vascular bundles. Spirotetramat is active against piercing-sucking insects, such as aphids, mites, and white flies, by acting as an ACC inhibitor, interrupting lipid biosynthesis in the insects. In Denmark, it is listed as harmful to aquatic invertebrates, but not dangerous to bees. Spirotetramat is possibly neutral. Bayer obtained spirotetramat's first regulatory approval in Tunisia in 2007. Spirotetramat (ISO Name) is a keto-enol insecticide developed by Bayer CropScience under the brand names Movento and Ultor. In plants, it is hydrolyzed to the enol form by cleavage of the central ethoxycarbonyl group. When tested on rats, it was not shown to be carcinogenic. Spirotetramat has moderate to low acute toxicity, is irritating to eyes and potentially sensitizing to skin. |
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| Structure | |
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| Synonyms | | Value | Source |
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| Movento | MeSH | | cis-4-(Ethoxycarbonyloxy)-8-methoxy-3-(2,5-xylyl)-1-azaspiro(4.5)dec-3-en-2-one | MeSH |
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| Chemical Formula | C21H27NO5 |
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| Average Molecular Weight | 373.449 |
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| Monoisotopic Molecular Weight | 373.188922973 |
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| IUPAC Name | 3-(2,5-dimethylphenyl)-2-hydroxy-8-methoxy-1-azaspiro[4.5]deca-1,3-dien-4-yl ethyl carbonate |
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| Traditional Name | 3-(2,5-dimethylphenyl)-2-hydroxy-8-methoxy-1-azaspiro[4.5]deca-1,3-dien-4-yl ethyl carbonate |
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| CAS Registry Number | Not Available |
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| SMILES | CCOC(=O)OC1=C(C(O)=NC11CCC(CC1)OC)C1=C(C)C=CC(C)=C1 |
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| InChI Identifier | InChI=1S/C21H27NO5/c1-5-26-20(24)27-18-17(16-12-13(2)6-7-14(16)3)19(23)22-21(18)10-8-15(25-4)9-11-21/h6-7,12,15H,5,8-11H2,1-4H3,(H,22,23) |
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| InChI Key | CLSVJBIHYWPGQY-UHFFFAOYSA-N |
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| Chemical Taxonomy |
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| Description | Belongs to the class of organic compounds known as p-xylenes. These are aromatic compounds that contain a p-xylene moiety, which is a monocyclic benzene carrying exactly two methyl groups at the 1- and 4-positions. |
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| Kingdom | Organic compounds |
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| Super Class | Benzenoids |
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| Class | Benzene and substituted derivatives |
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| Sub Class | Xylenes |
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| Direct Parent | p-Xylenes |
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| Alternative Parents | |
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| Substituents | - P-xylene
- Carbonic acid diester
- Enol ester
- Cyclic carboximidic acid
- Carbonic acid derivative
- Dialkyl ether
- Ether
- Propargyl-type 1,3-dipolar organic compound
- Organic 1,3-dipolar compound
- Organoheterocyclic compound
- Azacycle
- Organooxygen compound
- Organonitrogen compound
- Organopnictogen compound
- Carbonyl group
- Organic oxide
- Organic oxygen compound
- Organic nitrogen compound
- Hydrocarbon derivative
- Aromatic heteropolycyclic compound
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| Molecular Framework | Aromatic heteropolycyclic compounds |
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| External Descriptors | Not Available |
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| Ontology |
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|
Not Available | | Physical Properties |
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| State | Not Available |
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| Experimental Properties | | Property | Value | Reference |
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| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | logP | Not Available | Not Available |
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| Predicted Properties | [] |
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