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Cyclohexyl dimethylcarbamate is a chemical compound with the molecular formula C9H17NO2. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 44-46°C. cyclohexyl dimethylcarbamate is primarily used as an insecticide, specifically as a carbamate pesticide, which targets the nervous system of insects by inhibiting acetylcholinesterase, an enzyme essential for nerve impulse transmission. Cyclohexyl dimethylcarbamate is effective against a variety of pests, including aphids, mites, and whiteflies, and is often used in agriculture to protect crops. It is important to note that, like other carbamates, it should be handled with care due to its potential toxicity to humans and the environment, and it is subject to regulations regarding its use and disposal.

7541-19-7

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7541-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7541-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7541-19:
(6*7)+(5*5)+(4*4)+(3*1)+(2*1)+(1*9)=97
97 % 10 = 7
So 7541-19-7 is a valid CAS Registry Number.

7541-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexyl N,N-dimethylcarbamate

1.2 Other means of identification

Product number -
Other names N.N-Dimethyl-carbamidsaeure-cyclohexylester

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:7541-19-7 SDS

7541-19-7Downstream Products

7541-19-7Relevant academic research and scientific papers

Alkali-metal-assistent Transfer of the Carbamte Group from Phosphocarbamates to Alkyl Halides: a New Easy Way to Alkali-metal Carbamates and to Carbamate Esters

Aresta, Michele,Quaranta, Eugenio

, p. 1893 - 1900 (2007/10/02)

Phosphocarbamates P(O2CNR2)x(NR2)3-x (R=alkyl; x=1 or 2), easily obtainable by insertion of CO2 in the P-N bond of the corresponding aminophosphines P(NR2)3, have been used as a source of carbamate groups in the reaction with alkyl halides, R'X to afford carbamate esters.The reaction is mediated by alkali-metal halides, MY, and requires the presence of a suitable macrocyclic polyether (L).The overall reaction occurs in two steps: the carbamic group is first tranferred to the alkali-metal cation to give a carbamate salt which then reacts with the alkyl halide affording R2NC(O)OR'.The yield and selectivity to the carbamate ester are remarkably influenced by the nature of MY.The influence of the nature of the alkali-metal salt in the overall process and the role of the macrocyclic ligand in modifying the reactivity of the R2NCO2- anion in akli-metal carbamates are discussed.

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