1237740-64-5

Basic information

• Product Name: N-{3-[(E)-3-(4-ethoxyphenyl)acryloyl]-5-methyl-1,3,5-oxadiazinan-4-ylidene}nitramide
• Synonyms: N-{3-[(E)-3-(4-ethoxyphenyl)acryloyl]-5-methyl-1,3,5-oxadiazinan-4-ylidene}nitramide
• CAS NO: 1237740-64-5
• Molecular Weight: 334.332
• Mol File: 1237740-64-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-{3-[(E)-3-(4-ethoxyphenyl)acryloyl]-5-methyl-1,3,5-oxadiazinan-4-ylidene}nitramide(CAS DataBase Reference)
• NIST Chemistry Reference: N-{3-[(E)-3-(4-ethoxyphenyl)acryloyl]-5-methyl-1,3,5-oxadiazinan-4-ylidene}nitramide(1237740-64-5)
• EPA Substance Registry System: N-{3-[(E)-3-(4-ethoxyphenyl)acryloyl]-5-methyl-1,3,5-oxadiazinan-4-ylidene}nitramide(1237740-64-5)

Safety Data

• Hazardous Substances Data: 1237740-64-5(Hazardous Substances Data)

Upstream product

• 10031-82-0 4-ethoxybenzaldehyde 
• 77251-75-3 trans-p-ethoxycinnamoyl chloride 
• 153719-38-1 3,6-dihydro-3-methyl-N-nitro-2H-1,3,5-oxadiazin-4-amine 
• 2373-79-7 (E)-4-ethoxycinnamic acid 

Relevant articles and documents

Design, synthesis, and insecticidal activity of 1,5-diphenyl-1-pentanone analogues

Three series of novel 1,5-diphenyl-1-pentanone derivatives were designed and synthesized. Their structures were characterized by IR, 1H NMR techniques, and elemental analysis. The insecticidal activities of the new compounds were preliminarily evaluated. The bioassay results indicated that the compounds X11-X30 displayed better aphicidal activity against Aphis gossypii than compounds X1-X10 and the lead compound (E)-1,5-diphenyl-1-penten-1-one (A). The inhibitory rates of compounds X6 and X29 were 100% against Plutella xylostella (L.) at 600 mg·L-1. Compounds X12, X13, X19, X24, X25, X26 and X27 showed higher insecticidal activity against Tetranychus cinnabarinus (Boisduval) at 600 mg·L-1 than the lead compound (A).