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Beta-Carbaryl, also known as 1-naphthyl N-methylcarbamate, is a widely used synthetic carbamate insecticide that belongs to the carbamate class of chemicals. It is effective against a broad spectrum of pests, including insects, mites, and nematodes, and is commonly used in agriculture to protect crops from damage. Beta-Carbaryl works by inhibiting the acetylcholinesterase enzyme in the nervous system of pests, leading to their paralysis and eventual death. It is known for its relatively low toxicity to mammals and is considered a moderate-to-low risk pesticide when used according to label instructions. However, it is important to follow safety guidelines and regulations to minimize potential risks to human health and the environment.

4089-04-7

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4089-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4089-04-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4089-04:
(6*4)+(5*0)+(4*8)+(3*9)+(2*0)+(1*4)=87
87 % 10 = 7
So 4089-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c1-13-12(14)15-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3,(H,13,14)

4089-04-7SDS

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 naphthalen-2-yl N-methylcarbamate

1.2 Other means of identification

Product number -
Other names 2-Naphthyl-N-methylcarbamat

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:4089-04-7 SDS

4089-04-7Downstream Products

4089-04-7Relevant academic research and scientific papers

Ligand-assisted copper-catalyzed oxidative cross-coupling of simple phenols with formamides for the synthesis of carbamates

Reddy, Nagireddy Veera,Kumar, Gadde Sathish,Kumar, Pailla Santhosh,Kantam, M. Lakshmi,Reddy, Kallu Rajender

supporting information, p. 2133 - 2138 (2014/11/08)

An oxidative approach for the synthesis of phenyl carbamates has been achieved by ligand-assisted copper-catalyzed cross-dehydrogenative coupling (CDC) of phenols with formamides. The direct coupling of simple phenols with mono- and dialkyl formamides pro

Manufacture of α-naphthyl-N-methyl-carbamate

-

, (2008/06/13)

Process for the manufacture of N-alkyl and N-alkenyl carbamates by reacting a hydroxyl compound with a carbamyl chloride essentially free from phosgene and hydrogen chloride at a temperature of from 60° to 130° C in alkyl or halogen benzenes as solvent.

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