45829
Chlorpropham solution
100 μg/mL in acetonitrile, PESTANAL®, analytical standard
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About This Item
Empirical Formula (Hill Notation):
C10H12ClNO2
CAS Number:
Molecular Weight:
213.66
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
200-835-2
Beilstein/REAXYS Number:
2211397
MDL number:
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
concentration
100 μg/mL in acetonitrile
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
agriculture
format
single component solution
storage temp.
2-8°C
SMILES string
CC(C)OC(=O)Nc1cccc(Cl)c1
InChI
1S/C10H12ClNO2/c1-7(2)14-10(13)12-9-5-3-4-8(11)6-9/h3-7H,1-2H3,(H,12,13)
InChI key
CWJSHJJYOPWUGX-UHFFFAOYSA-N
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
35.6 °F - closed cup
flash_point_c
2 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Christine Mara et al.
Bioorganic & medicinal chemistry letters, 21(20), 6180-6183 (2011-09-06)
A series of phosphoramidate and phosphorothioamidate compounds based on the lead antitubulin herbicidal agents amiprophos methyl (APM) and butamifos were synthesised and evaluated for antimalarial activity. Of these compounds, phosphorothioamidates were more active than their oxo congeners and the nature
Fabien Vincent et al.
Bioorganic & medicinal chemistry letters, 19(23), 6793-6796 (2009-10-24)
The screening of known medicinal agents against new biological targets has been shown to be a valuable approach for revealing new pharmacology of marketed compounds. Recently, carbamate, urea and ketone inhibitors of fatty acid amide hydrolase (FAAH) have been described