112225-87-3

Basic information

• Product Name: 1,2-DIBENZOYL-1-(T-BUTYL)HYDRAZINE
• Synonyms: RH5849;benzoicacid,2-benzoyl-1-(1,1-dimethylethyl)hydrazide;1,2-DIBENZOYL-1-(T-BUTYL)HYDRAZINE;1,2-DIBENZOYL-1-TERT-BUTYLHYDRAZINE W.P.;1,2-dibenzoyl-tert-butylhydrazine;2BENZOYL1TERTBUTYLBENZOYLHYDRAZINE;1,2-Dibenzoyl-1-tert-butylhydrazine;Benzoic acid 2-benzoyl-1-tert-butyl hydrazide
• CAS NO: 112225-87-3
• Molecular Formula: C₁₈H₂₀N₂O₂
• Molecular Weight: 296.36
• Mol File: 112225-87-3.mol
• Article Data: 12

Chemical Properties

• Melting Point: 178.5 °C
• Appearance: /
• Density: 1.128 g/cm³
• Refractive Index: 1.577
• PKA: 10.97±0.46(Predicted)
• CAS DataBase Reference: 1,2-DIBENZOYL-1-(T-BUTYL)HYDRAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DIBENZOYL-1-(T-BUTYL)HYDRAZINE(112225-87-3)
• EPA Substance Registry System: 1,2-DIBENZOYL-1-(T-BUTYL)HYDRAZINE(112225-87-3)

Safety Data

• Hazardous Substances Data: 112225-87-3(Hazardous Substances Data)

Usage

Uses

1,2-Dibenzoyl-1-(tert-butyl)hydrazine is an ecdysone agonist that causes the premature initiation of molting at all stages of larval development of the tobacco hornworm, Manduca sexta.

InChI:InChI=1/C18H20N2O2/c1-18(2,3)20(17(22)15-12-8-5-9-13-15)19-16(21)14-10-6-4-7-11-14/h4-13H,1-3H3,(H,19,21)

Upstream product

• 32154-73-7 tert-butylhydrazine oxalate 
• 98-88-4 benzoyl chloride 
• 99981-48-3 N'-t-butyl-N'-benzoylhydrazine 
• 17473-79-9 1-benzoyl-2-tert-butylhydrazine 
• 7400-27-3 tertbutylhydrazine hydrochloride 

Downstream Products

• 857505-17-0 C₁₈H₁₉ClN₂O₂S 
• 115154-99-9 N-methylthiomethyl-N'-t-butyl-N,N'-dibenzoylhydrazine 
• 115154-97-7 N-allyl-N'-t-butyl-N,N'-dibenzoylhydrazine 
• 115154-98-8 N-methoxymethyl-N'-t-butyl-N-N'-dibenzoylhydrazine 
• 115154-96-6 N-benzyl-N'-t-butyl-N,N'-dibenzoylhydrazine 
• 65715-09-5 2-phenyl-3-benzoyl-1,3,4-oxadiazole-2-(3H)-thione 
• 57064-92-3 3-benzoyl-5-phenyl-3H-[1,3,4]-oxadiazol-2-one 
• 5894-65-5 N-t-butylbenzamide 

Relevant articles and documents

Synthesis and insecticidal evaluation of novel N-(S-amino)sulfenylated derivatives of diacylhydrazines

A series of new N-(S-amino)sulfenylated derivatives of diacylhydrazines were synthesized by the reaction of S-aminosulfenyl chlorides with N-tert-butyl-N′-benzoyl-N-substituted benzoylhydrazines in the presence of sodium hydride, and evaluated for moulting hormone mimicking activity. In the course of syntheses, N - N bond cleavage in diacylhydrazines was found and the reaction was studied in some detail. The results of bioassay showed that the title compounds exhibit excellent larvicidal activity. Toxicity assays indicated that these compounds can induce a premature, abnormal and lethal larval mount.

Synthesis and biological activity of novel N-sulfenylated derivatives of diacylhydrazines

A series of new N-sulfenylated derivatives of diacylhydrazines were synthesised and evaluated for moulting hormone mimicking activity, and the results of bioassay showed that the title compounds exhibit excellent larvicidal activities, and toxicity assays

Insecticidal N'-substituted-N,N'-disubstitutedhydrazines

This invention relates to N'-substituted-N,N'-disubstitutedhydrazines of formula I wherein X and X' are independently O, S, or NR; A' and B' are independently substituted or unsubstituted aryl or aromatic heterocycle; wherein F is alkyl, alkenyl, or aralkyl; and wherein E is a tertiary carbon containing organic radical having a total of at least four carbon and halogen atoms but not more than six halogen atoms, or a non-tertiary carbon containing non-haloalkyl organic or organometallic radical having at least five atoms other than hydrogen, oxygen and halogen which are useful as insecticides, compositions containing those compounds, methods of producing the compounds, and methods of their use. More particularly, the invention relates to insect growth regulating compounds and compositions, and methods of using such compounds and compositions. Compounds of the present invention are particularly suitable for controlling plant-destructive insects in crops of cultivated plants, ornamentals and forestry.