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Basic information

  • Name:
  • Benzamide,2-chloro-N-[[[4-(trifluoromethoxy)phenyl]amino]carbonyl]-

  • Superlist Name:
  • Triflumuron
  • CAS No.:
  • 64628-44-0

  • Formula:
  • C15H10ClF3N2O3
  • Synonyms:
  • 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea;Alsystin;Alsystine;BAY-SIR 8514;BAY-Vi 7533;Baycidal;N-(2-Chlorobenzoyl)-N'-[4-(trifluoromethoxy)phenyl]urea;OMS 2015;SIR 8514;Starycide;Trifluron;2-Chloro-N-{[4-(trifluoromethoxy)phenyl]carbamoyl}benzamide;
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Consensus Reports

Stability:Stable at normal temperatures and pressures.
First Aid Measures:
Ingestion:If swallowed, wash out mouth with water provided person is conscious. Call a physician.
Inhalation: If inhaled, remove to fresh air. If breathing becomes difficult, call a physician.
Skin: In case of contact, immediately wash skin with soap and copious amounts of water.
Eyes:In case of contact with eyes, flush with copious amounts of water for at least 15 minutes. Assure adequate flushing by separating the eyelids with fingers. Call a physician.

Specification

The Triflumuron, with the CAS registry number 64628-44-0 and EINECS registry number 264-980-3, has the systematic name of 2-chloro-N-{[4-(trifluoromethoxy)phenyl]carbamoyl}benzamide. And the molecular formula of this chemical is C15H10ClF3N2O3. What's more, while dealing with this chemical, you should not breathe dust and then try to avoid contacting with skin and eyes. In addition, it should be stored at 0-6°C.

The physical properties of Triflumuron are as following: (1)ACD/LogP: 4.55; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 4.55; (4)ACD/LogD (pH 7.4): 4.53; (5)ACD/BCF (pH 5.5): 1683.26; (6)ACD/BCF (pH 7.4): 1630.29; (7)ACD/KOC (pH 5.5): 7092.94; (8)ACD/KOC (pH 7.4): 6869.72; (9)#H bond acceptors: 5; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 49.85 Å2; (13)Index of Refraction: 1.581; (14)Molar Refractivity: 81.11 cm3; (15)Molar Volume: 243 cm3; (16)Polarizability: 32.15×10-24cm3; (17)Surface Tension: 46.8 dyne/cm; (18)Density: 1.475 g/cm3.

Preparation and uses of Triflumuron: It can be prepared by 2 - chlorobenzoyl isocyanate and 4-(trifluoromethoxy)aniline refluxing in benzene. What's more, it is used as insect growth inhibitor for the control of psyllidae, lepidoptera and coleoptera insects.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C(c1ccccc1Cl)NC(=O)Nc2ccc(OC(F)(F)F)cc2
(2)InChI: InChI=1/C15H10ClF3N2O3/c16-12-4-2-1-3-11(12)13(22)21-14(23)20-9-5-7-10(8-6-9)24-15(17,18)19/h1-8H,(H2,20,21,22,23)
(3)InChIKey: XAIPTRIXGHTTNT-UHFFFAOYAH

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