| Weight | 179.219 g/mol |
|---|---|
| Formula | C10H13NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Propham (122-42-9)
isopropyl N-phenylcarbamate · Merck 4925 · Merck-4925
Score:
#10 in Molecular and cellular biology
,
#407 in Biochemistry
,
#1387 in Biology
,
#1622 in Chemistry
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- Effects of cold and of isopropyl-N-phenylcarbamate on the second meiotic spindle of mouse oocytes. (European Journal of Cell Biology, 1980)
- Comparison of trifluralin, oryzalin, pronamide, propham, and colchicine treatments on microtubules (Pesticide Biochemistry and Physiology, 1973)
- Propham mineralization in aqueous medium by anodic oxidation using boron-doped diamond anode : Influence of experimental parameters on degradation kinetics and mineralization efficiency (Water Research, 2008)
- Isopropyl N-Phenylcarbamate Affects Spindle Microtubule Orientation in Dividing Endosperm Cells of Haemanthus Katherinae Baker (Journal of Cell Science, 1969)
- A comparative study on the efficiency of electro-Fenton process in the removal of propham from water (Applied Catalysis B-environmental, 2009)
- Determination of imidacloprid, metalaxyl, myclobutanil, propham, and thiabendazole in fruits and vegetables by liquid chromatographyatmospheric pressure chemical ionizationmass spectrometry (Fresenius Journal of Analytical Chemistry, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - isopropyl N-phenylcarbamate
- Merck 4925
- Merck-4925
-
SMILESCC(C)OC(=O)NC1=CC=CC=C1
-
InChIKeyVXPLXMJHHKHSOA-UHFFFAOYSA-N
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