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Tert-butyl (3-methyl-4-nitrophenyl)carbamate is a carbamate derivative chemical compound characterized by the presence of a tert-butyl group attached to a 3-methyl-4-nitrophenyl group. This structural feature endows the compound with both stability and efficacy in pest control, making it a widely used agent in agricultural applications.

1380445-45-3

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1380445-45-3 Usage

Uses

Used in Agricultural Applications:
Tert-butyl (3-methyl-4-nitrophenyl)carbamate is used as a pesticide and insecticide for controlling a broad spectrum of pests and insects. Its application reason is attributed to its ability to effectively manage various types of pests, thereby protecting crops and ensuring agricultural productivity.
However, due to its potential toxicity to humans and the environment, it is crucial to exercise proper precautions when handling and applying tert-butyl (3-methyl-4-nitrophenyl)carbamate. This includes adhering to safety guidelines and regulations to minimize risks and ensure the sustainable use of tert-butyl (3-methyl-4-nitrophenyl)carbamate in agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 1380445-45-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,4,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1380445-45:
(9*1)+(8*3)+(7*8)+(6*0)+(5*4)+(4*4)+(3*5)+(2*4)+(1*5)=153
153 % 10 = 3
So 1380445-45-3 is a valid CAS Registry Number.

1380445-45-3Relevant academic research and scientific papers

Methaqualone hapten as well as synthesis method and application thereof

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Paragraph 0055-0057; 0064-0065; 0072-0073, (2020/05/01)

The invention discloses a methaqualone hapten as well as a synthesis method and application thereof. The synthesis method comprises the following steps: protecting amino of 3-methyl-4-nitroaniline byusing di-tert-butyl dicarbonate to obtain a product inte

MOLECULES HAVEING PESTICIDAL UTILIY AND INTERMEDIATES, COMPOSITIONS AND PROCESSES RELATED THERETO

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Paragraph 1732-1733, (2018/04/20)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

Synthesis of amino-substituted indoles using the Bartoli reaction

Wylie, Laura,Innocenti, Paolo,Whelligan, Daniel K.,Hoelder, Swen

supporting information; experimental part, p. 4441 - 4447 (2012/06/30)

We report herein the concise preparation of a range of functionalised aminoindoles via a new application of the Bartoli reaction. Scope and limitations of the methodology have been extensively studied to reveal the importance of protecting groups and subs

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