Etoxazole

Chemodex
Product Code: CDX-E0064
Product Group: Other Biochemicals
Supplier: Chemodex
CodeSizePrice
CDX-E0064-M100100 mg£157.00
Quantity:
CDX-E0064-M250250 mg£304.00
Quantity:
CDX-E0064-G0011 g£890.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
Ambient
Storage:
+20°C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Alternate Names/Synonyms:
(RS)-5-tert-Butyl-2-[2-(2,6-difluorophenyl)-4,5-dihydro-1,3-oxazol-4-yl]phenetole; 4-(4-tert-Butyl-2-ethoxyphenyl)-2-(2,6-difluorophenyl)-4,5-dihydrooxazole
Appearance:
White to off-white powder.
CAS:
153233-91-1
Class:
9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07,GHS09
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H332, H410
InChi:
InChI=1S/C21H23F2NO2/c1-5-25-18-11-13(21(2,3)4)9-10-14(18)17-12-26-20(24-17)19-15(22)7-6-8-16(19)23/h6-11,17H,5,12H2,1-4H3
InChiKey:
IXSZQYVWNJNRAL-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 153233-91-1. Formula: C21H23F2NO2. MW: 359.4. Synthetic. Acaricide/Insecticide. Mode of action is via chitin biosynthesis inhibition for the control of mites. Compound can be used as analytical reference material.
MDL:
MFCD07363987
Molecular Formula:
C21H23F2NO2
Molecular Weight:
359.4
Package Type:
Vial
Precautions:
P261, P273, P304, P340, P312, P391, P501
Product Description:
Acaricide/Insecticide. Mode of action is via chitin biosynthesis inhibition for the control of mites. Compound can be used as analytical reference material.
Purity:
>99% (HPLC)
Signal word:
Warning
SMILES:
CC(C1=CC=C(C2N=C(C3=C(F)C=CC=C3F)OC2)C(OCC)=C1)(C)C
Solubility Chemicals:
Soluble in chloroform, ethyl acetate or methanol. Insoluble in water.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UN Nummer:
UN 3077
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.

References

(1) R. Nauen & G. Smagghe; Pest Manag. Sci. 62, 379 (2006) | (2) P. Demaeght, et al.; Insect. Biochem. Mol. Biol. 51, 52 (2014)

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