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DIBUTYL AMIDOSULFENYL CHLORIDE is an organic compound that serves as a reagent in the synthesis of various chemical products, particularly in the preparation of pesticides.

6541-82-8

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6541-82-8 Usage

Uses

Used in Pesticide Industry:
DIBUTYL AMIDOSULFENYL CHLORIDE is used as a reagent for the preparation of pesticides. It plays a crucial role in the synthesis of active ingredients that help control, repel, or kill pests such as insects, weeds, and fungi, thereby protecting crops and enhancing agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 6541-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6541-82:
(6*6)+(5*5)+(4*4)+(3*1)+(2*8)+(1*2)=98
98 % 10 = 8
So 6541-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H18ClNS/c1-3-5-7-10(11-9)8-6-4-2/h3-8H2,1-2H3

6541-82-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (dibutylamino) thiohypochlorite

1.2 Other means of identification

Product number -
Other names Amidosulfenyl chloride,dibutyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6541-82-8 SDS

6541-82-8Downstream Products

6541-82-8Relevant academic research and scientific papers

Preparation method of carbofuran derivatives

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Paragraph 0043; 0046; 0049; 0052, (2017/08/29)

The invention discloses a preparation method of carbofuran derivatives. The preparation method of the carbofuran derivatives comprises the following steps: (1) taking amine derivatives and sulfur monochloride as raw materials, adding a first acid-binding agent and a reaction solvent and performing sulfuration reaction to obtain a first intermediate disulfide, wherein the first acid-binding agent is triethylamine and the reaction solvent is chloroform or dichloromethane; (2) performing chlorination reaction on the first intermediate disulfide and chlorine which serve as raw materials to obtain a second intermediate nitrogen and sulfur chloride; (3) taking the second intermediate nitrogen and sulfur chloride and carbofuran as raw materials, adding a second acid-binding agent and performing condensation reaction to obtain the carbofuran derivatives. The preparation method has the advantages that the process is simple, and the product is low in toxicity, high in purity and high in yield.

Synthesis and insecticidal evaluation of novel N-(S-amino)sulfenylated derivatives of diacylhydrazines

Wang, Qingmin,Cheng, Junran,Huang, Runqin

, p. 1250 - 1253 (2007/10/03)

A series of new N-(S-amino)sulfenylated derivatives of diacylhydrazines were synthesized by the reaction of S-aminosulfenyl chlorides with N-tert-butyl-N′-benzoyl-N-substituted benzoylhydrazines in the presence of sodium hydride, and evaluated for moulting hormone mimicking activity. In the course of syntheses, N - N bond cleavage in diacylhydrazines was found and the reaction was studied in some detail. The results of bioassay showed that the title compounds exhibit excellent larvicidal activity. Toxicity assays indicated that these compounds can induce a premature, abnormal and lethal larval mount.

N-sulfenylated pyrazolines, compositions and use

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, (2008/06/13)

N-sulfenylated and N-acrylated pyrazoline arthropodicides, compositions containing them and methods for controlling arthropods by applying compounds of the invention to them or to their environment. The pyrazolines are selected from those of Formulae I to III wherein R1, R2, R3, Q, A, B, J, K, Y, m, n and p are as defined in the test: STR1

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