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2-(Propylthio)phenyl methylcarbamate is a chemical compound with the molecular formula C11H15NOS2. It is an organosulfur compound and a member of the carbamate family, which are known for their use as pesticides and insecticides. This specific compound features a phenyl ring with a propylthio group attached at the 2-position and a methylcarbamate group at the para position. The propylthio group provides a sulfur-containing alkyl chain, which can enhance the compound's lipophilicity and potentially its biological activity. The methylcarbamate group is a common structural motif in many pesticides, known for its ability to inhibit acetylcholinesterase, an enzyme crucial for nerve impulse transmission. This inhibition can lead to the disruption of the nervous system in insects, making 2-(propylthio)phenyl methylcarbamate a potentially effective agent against certain pests. However, the specific use, efficacy, and safety profile of 2-(propylthio)phenyl methylcarbamate would require further investigation and testing to determine its practical applications and any associated risks.

4559-15-3

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4559-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4559-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4559-15:
(6*4)+(5*5)+(4*5)+(3*9)+(2*1)+(1*5)=103
103 % 10 = 3
So 4559-15-3 is a valid CAS Registry Number.

4559-15-3Downstream Products

4559-15-3Relevant academic research and scientific papers

Mosquito acetylcholinesterase as a target for novel phenyl-substituted carbamates

Mutunga, James M.,Ma, Ming,Chen, Qiao-Hong,Hartsel, Joshua A.,Wong, Dawn M.,Ding, Sha,Totrov, Max,Carlier, Paul R.,Bloomquist, Jeffrey R.

, (2019)

New insecticides are needed for control of disease-vectoring mosquitoes and this research evaluates the activity of new carbamate acetylcholinesterase (AChE) inhibitors. Biochemical and toxicological characterization of carbamates based on the parent stru

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