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(2-(morpholin-4-yl)ethyl)carbamic acid 2,2,2-trifluoroethyl ester is an ester derivative of carbamic acid and 2,2,2-trifluoroethanol, commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.

1197808-29-9

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1197808-29-9 Usage

Uses

Used in Agrochemical Industry:
(2-(morpholin-4-yl)ethyl)carbamic acid 2,2,2-trifluoroethyl ester is used as a pesticide, herbicide, or fungicide for its ability to inhibit specific enzymes or processes in target organisms.
Used in Pharmaceutical Industry:
(2-(morpholin-4-yl)ethyl)carbamic acid 2,2,2-trifluoroethyl ester is used as a precursor to create new drugs or therapeutic compounds.
Note: Further research and testing are needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1197808-29-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,8,0 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1197808-29:
(9*1)+(8*1)+(7*9)+(6*7)+(5*8)+(4*0)+(3*8)+(2*2)+(1*9)=199
199 % 10 = 9
So 1197808-29-9 is a valid CAS Registry Number.

1197808-29-9Downstream Products

1197808-29-9Relevant academic research and scientific papers

A facile synthesis of unsymmetrical ureas

Bogolubsky, Andrey V.,Ryabukhin, Sergey V.,Pipko, Sergey E.,Lukin, Oleg,Shivanyuk, Alexander,Mykytenko, Dmytro,Tolmachev, Andrey

experimental part, p. 3619 - 3623 (2011/06/21)

A facile and versatile method for the synthesis of unsymmetrical ureas from readily available reagents is reported. In the first step trifluoroethylchloroformate is reacted with a stoichiometric amount of a primary amine to give an intermediate trifluoroethyl carbamate. The addition of a second amine (primary or secondary) to the trifluoroethyl carbamate furnishes corresponding unsymmetrical ureas in 75-85% yield. A simple workup procedure, the high yields obtained, and the purity of the isolated products are suitable for the parallel synthesis of combinatorial libraries of unsymmetrical ureas with high structural and functional diversity.

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