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Carbamic acid, (5-methyl-3-isoxazolyl)-, 1,1-dimethylethyl ester (9CI), commonly known as carbaryl, is a white crystalline solid that functions as a potent insecticide. It is highly toxic to insects and pests, inhibiting the activity of the enzyme cholinesterase, which results in paralysis and death of the target organisms. Despite its effectiveness, it is considered moderately toxic to humans and can have adverse environmental impacts, leading to certain restrictions on its use.

97517-66-3

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97517-66-3 Usage

Uses

Used in Agricultural Industry:
Carbamic acid, (5-methyl-3-isoxazolyl)-, 1,1-dimethylethyl ester (9CI) is used as an insecticide for protecting crops from various pests. Its application helps to ensure the health and yield of agricultural produce by reducing the damage caused by insects.
Used in Residential Pest Control:
In residential settings, carbaryl is used as a pest control agent to manage and eliminate insect infestations. It is particularly useful in controlling household pests such as cockroaches and ants, contributing to a cleaner and healthier living environment.
However, due to its moderate toxicity to humans and potential environmental harm, the use of carbaryl is subject to regulations and restrictions in certain regions to minimize risks to human health and ecological balance.

Check Digit Verification of cas no

The CAS Registry Mumber 97517-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,1 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97517-66:
(7*9)+(6*7)+(5*5)+(4*1)+(3*7)+(2*6)+(1*6)=173
173 % 10 = 3
So 97517-66-3 is a valid CAS Registry Number.

97517-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(5-methyl-1,2-oxazol-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names QC-1021

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:97517-66-3 SDS

97517-66-3Relevant academic research and scientific papers

TRICYCLIC SPIROCYCLE DERIVATIVES AND METHODS OF USE

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Page/Page column 47, (2011/07/29)

The present invention relates to novel Tricyclic Spirocycle Derivatives, pharmaceutical compositions comprising the Tricyclic Spirocycle Derivatives and the use of these compounds for treating or preventing allergy, an allergy-induced airway response, congestion, a cardiovascular disease, an inflammatory disease, a gastrointestinal disorder, a neurological disorder, a metabolic disorder, obesity or an obesity-related disorder, diabetes, a diabetic complication, impaired glucose tolerance or aired fasting glucose.

NOVEL DUAL ACTION RECEPTORS ANTAGONISTS (DARA) AT THE AT1 AND ETA RECEPTORS

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Page/Page column 34-35; 45-46; 56-57; 66-67; 74; 84; 92; 103-104, (2010/11/28)

The present invention relates to new compounds of the formula [Chemical formula should be inserted here. Please see paper copy] wherein R1, R2, R3, and R31 are as specified herein. The invention also relates to a method for preparation thereof, as well as combinations of the new compounds with previously known agents. The invention also relates to the use of the above-mentioned compounds and combinations for the preparation of a medicament for treating hypertension of different kinds, alleviating organ damage of different kinds, treating or preventing diabetic nephropathy, treating endothelin and angiotensin mediated disorders, and treating prostate cancer.

HETEROCYCLIC COMPOUNDS

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Page/Page column 46, (2008/06/13)

New compounds of formula (I), wherein the meanings for the various substituents are as disclosed in the description. These compounds are useful as p38 kinase inhibitors.

Directed lithiation of N-(tert-butoxycarbonyl)aminoisoxazole: Synthesis of 4-substituted aminoisoxazoles

Konoike, Toshiro,Kanda, Yasuhiko,Araki, Yoshitaka

, p. 3339 - 3342 (2007/10/03)

Directed lithiation of 3-(Boc-amino)isoxazole 4 and 5-(Boc-amino)isoxazole 9 is described. Dilithioisoxazoles reacted with a variety of electrophiles to give the corresponding 4-substituted isoxazoles.

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