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Rotenone isooxime is a chemical compound derived from the natural compound rotenone, which is extracted from the roots of certain plants. It is used as a pesticide and insecticide, acting as a contact and stomach poison for insects and pests. Rotenone isooxime disrupts the nervous system of insects, causing paralysis and death.

6544-83-8

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6544-83-8 Usage

Uses

Used in Agriculture:
Rotenone isooxime is used as a pesticide for controlling pests on crops. It helps protect crops from damage caused by insects and pests, ensuring a healthy and productive yield.
Used in Forestry:
In the forestry industry, rotenone isooxime is used as an insecticide to protect trees from insect damage. It helps maintain the health and longevity of trees, preventing the spread of diseases and infestations.
However, it is important to note that due to the potential negative impact of rotenone isooxime on non-target organisms and the environment, its use is carefully regulated in many countries. This regulation aims to minimize the risks associated with its application while still benefiting from its pest control properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6544-83-8 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 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6544-83:
(6*6)+(5*5)+(4*4)+(3*4)+(2*8)+(1*3)=108
108 % 10 = 8
So 6544-83-8 is a valid CAS Registry Number.

6544-83-8SDS

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 rotenone-iso oxime

1.2 Other means of identification

Product number -
Other names 5-(7,8-Dimethoxy-3a,9b-dihydro-4H-chromeno[4,3-d]isoxazol-1-yl)-2-isopropenyl-2,3-dihydro-benzofuran-4-ol

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:6544-83-8 SDS

6544-83-8Relevant academic research and scientific papers

Reactions of Rotenoids with Hydroxylamine

Kostova, Ivanka

, p. 195 - 198 (2007/10/02)

Reaction of rotenone (1a) and amorphigenin (2a) with hydroxylamine in alkaline medium affords a mixture of the isoximes 5 and 6, and the new 6a-NH2 spiro derivatives 12a, b and 13a, b.The structures, stereochemistry, and the mechanism of formation of these products are discussed.

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