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O-Octyl-S-(4-brom-phenacyl)-dithiocarbonat, also known as 4-bromophenacyl octyl dithiocarbamate, is a chemical compound with the molecular formula C17H24BrNOS2. It is a derivative of dithiocarbamic acid, featuring an octyl group and a 4-bromophenacyl group attached to the sulfur atoms. O-Octyl-S-(4-brom-phenacyl)-dithiocarbonat is primarily used as a pesticide, fungicide, and herbicide, exhibiting protective, curative, and eradicant properties. It is effective against a wide range of pests, diseases, and weeds, making it a valuable tool in agriculture and horticulture. The compound's mode of action involves inhibiting various enzymes and disrupting the metabolic processes of target organisms, leading to their death. Due to its broad-spectrum activity and effectiveness, O-Octyl-S-(4-brom-phenacyl)-dithiocarbonat plays a significant role in crop protection and yield enhancement.

3756-06-7

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3756-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3756-06-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3756-06:
(6*3)+(5*7)+(4*5)+(3*6)+(2*0)+(1*6)=97
97 % 10 = 7
So 3756-06-7 is a valid CAS Registry Number.

3756-06-7Downstream Products

3756-06-7Relevant academic research and scientific papers

SYNTEZY ZWIAZKOW O POTENCJALNYM DZIALANIU RADIOUCZULAJACYM. VIII. SYNTEZY ALKILOKSANTOGENIANOW 4-CHLORO- I 4-BROMOFENACYLOWYCH

Skwarski, Dionizy,Sobolewski, Henryk

, p. 213 - 218 (2007/10/02)

In the frame-work of search for new potential radiosensitizers a series of novel 4-chloro- and 4-bromophenacyl alkylxanthates were synthetized by reacting 4-chloro- and 4-bromophenacyl bromide with potassium alkylxanthates, in which allyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, isopentyl, heksyl, heptyl, octyl, isooctyl, decyl, 3-tetrahydrofurfuryl, benzyl, phenylethyl and phenylpropyl constituted the alkyl group.

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