chromafenozide
N-tert-butyl-N'-(3,5-dimethylbenzoyl)-5-methylchromane-6-carbohydrazide
Identification
| Name | chromafenozide |
| CAS Number | 143807-66-3 |
| FDA UNII | 2ODM465D5M |
| Molecular Formula | C24 H30 N2 O3 |
| Molecular Weight | 394.51470000 |
| MDL Number | MFCD28015761 |
| Nikkaji Number | J1.295.632K |
| Beilstein | 10113703 |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Flash Point | 32.00 °F. TCC ( 0.00 °C. ) (est) |
| logP (o/w) | 4.510 (est) |
| Soluble in | water, 0.5763 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | herbicides / pesticides |
| Recommendation for chromafenozide usage levels up to | not for fragrance use. |
| Recommendation for chromafenozide flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
2H-1-
benzopyran-6-carboxylic acid, 3,4-dihydro-5-methyl-, 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide
N'-tert-
butyl-N'-(3,5-dimethylbenzoyl)-5-methyl-3,4-dihydro-2H-chromen-6-carbohydrazid
N'-tert-
butyl-N'-(3,5-dimethylbenzoyl)-5-methyl-3,4-dihydro-2H-chromene-6-carbohydrazide
N-tert-
butyl-N'-(3,5-dimethylbenzoyl)-5-methylchromane-6-carbohydrazide
3,4-
dihydro-5-methyl-2H-1-benzopyran-6-carboxylic acid 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide
N'-(3,5-
dimethylbenzoyl)-5-methyl-N'-(2-methyl-2-propanyl)-6-chromanecarbohydrazide
PubMed:
Residues, dissipation and safety evaluation of chromafenozide in strawberry under open field conditions.
PubMed:
HPLC method development and validation of chromafenozide in paddy.
PubMed:
Degradation dynamics of chromafenozide in different types of soil.
PubMed:
Determination of 16 insect growth regulators in edible Chinese traditional herbs by liquid chromatography electrospray tandem mass spectrometry.
PubMed:
Development of an in vitro binding assay for ecdysone receptor of mysid shrimp (Americamysis bahia).
PubMed:
Residue analysis of four diacylhydrazine insecticides in fruits and vegetables by Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method using ultra-performance liquid chromatography coupled to tandem mass spectrometry.
PubMed:
[Determination of five diacylhydrazine insecticide residues in welsh onion using high performance liquid chromatography-tandem mass spectrometry].
PubMed:
Towards Coleoptera-specific high-throughput screening systems for compounds with ecdysone activity: development of EcR reporter assays using weevil (Anthonomus grandis)-derived cell lines and in silico analysis of ligand binding to A. grandis EcR ligand-binding pocket.
PubMed:
QSAR and mode of action studies of insecticidal ecdysone agonists.
PubMed:
Nonsteroidal ecdysone agonists.
PubMed:
Classical and three-dimensional QSAR for the inhibition of [3H]ponasterone A binding by diacylhydrazine-type ecdysone agonists to insect Sf-9 cells.
PubMed:
Binding mode of ecdysone agonists to the receptor: comparative modeling and docking studies.
PubMed:
Synthesis and insecticidal activity of benzoheterocyclic analogues of N'-benzoyl-N-(tert-butyl)benzohydrazide: Part 3. Modification of N-tert-butylhydrazine moiety.
PubMed:
Potent and selective partial ecdysone agonist activity of chromafenozide in Sf9 cells.