chromafenozide

N-tert-butyl-N'-(3,5-dimethylbenzoyl)-5-methylchromane-6-carbohydrazide

CAS: 143807-66-3 C24 H30 N2 O3 MW: 394.51470000

Identification

Namechromafenozide
CAS Number143807-66-3
FDA UNII2ODM465D5M
Molecular FormulaC24 H30 N2 O3
Molecular Weight394.51470000
MDL NumberMFCD28015761
Nikkaji NumberJ1.295.632K
Beilstein10113703

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 ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryherbicides / pesticides
Recommendation for chromafenozide usage levels up tonot for fragrance use.
Recommendation for chromafenozide flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

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.