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OXADIARGYL PESTANAL

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OXADIARGYL PESTANAL Basic information

Product Name:
OXADIARGYL PESTANAL
Synonyms:
  • 3-[2,4-dichloro-5-(2-propynyloxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2(3H)-one
  • 5-tert-butyl-3-(2,4-dichloro-5-(prop-2-ynyloxy)phenyl)-1,3,4-oxadiazol-2-(3H)-one
  • Raft
  • Topstar
  • 3,5,6-Trichloro-2-pyridinol, Pestanal
  • oxadiargyl (pa iso)
  • 1,3,4-Oxadiazol-2(3H)-one, 3-(2,4-dichloro-5-(2-propynyloxy)phenyl)-5- (1,1-dimethylethyl)-
  • OXADIARGYL STANDARD
CAS:
39807-15-3
MF:
C15H14Cl2N2O3
MW:
341.19
EINECS:
254-637-6
Product Categories:
  • Agro-Products
  • Aromatics
  • Heterocycles
Mol File:
39807-15-3.mol
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OXADIARGYL PESTANAL Chemical Properties

Melting point:
131℃
Boiling point:
429.6±55.0 °C(Predicted)
Density 
1.29±0.1 g/cm3(Predicted)
solubility 
Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Solid
pka
-2.99±0.40(Predicted)
color 
Off-white to light brown
Stability:
Stable under recommended storage conditions., Stable Under Recommended Storage C
LogP
3.950
EPA Substance Registry System
1,3,4-Oxadiazol-2(3H)-one, 3-[2,4-dichloro-5-(2-propynyloxy)phenyl]-5-(1,1-dimethylethyl)- (39807-15-3)
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Safety Information

Hazard Codes 
Xn,N
Risk Statements 
48/22-63-50/53
Safety Statements 
36/37-46-60-61
RIDADR 
UN3077 9/PG 3
WGK Germany 
3
RTECS 
RO0907700
HS Code 
29349990
Toxicity
LD50 in rats (mg/kg): >5000 orally; >2000 dermally; LC50 (4 hr) in rats: >5.16 mg/l (Dickmann)
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OXADIARGYL PESTANAL Usage And Synthesis

Uses

Oxadiargyl is pre-emergence herbicide for use in rice and other food crops.

Uses

Herbicide.

Hazard

A reproductive hazard.

Synthesis

1. 2,4-Dichlorophenol, hydrazine hydrate, and propargyl chloride were used as the main raw materials, and propargyl oxacillin was synthesized by a six-step reaction including nitration, reduction, diazotization, acylation, cyclization, and etherification, with an overall yield of 35.5%.

2. 2,4-Dioxophenol was used as the starting material. After etherification, nitration, reduction to produce intermediate substituted aniline; then acylation, and finally with phosgene ring is obtained.

3. The hydrolysis of oxacillin is used to obtain oxacillinol, and then oxacillinol in the presence of polar solvent C2 ~ C5 fatty alcohols, inorganic alkali as the acid-binding agent, in the role of the catalyst, under 0.1 ~ 0.4MPa alkylation reaction to produce propargyl oxacillinol alcohol solution, and then filtration, washing, removal of some of the polar solvent C2 ~ C5 fat alcohols at negative pressure, crystallization and filtration, cooling, Drying to get propargyl oxazolone.

OXADIARGYL PESTANALSupplier

J & K SCIENTIFIC LTD.
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18210857532; 18210857532
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021-50135380
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