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Trifluoromethanesulfonic acid 4-(2-tert-butoxyethoxy)-6-(4-tert-butylbenzenesulfonylamino)-5-(2-methoxyphenoxy)pyrimidin-2-yl ester is a complex chemical compound known for its unique properties and wide range of applications in various industries. It is characterized by its ability to act as a strong acid catalyst in organic synthesis reactions, which is attributed to its multiple functional groups, including an ethoxyethoxy side chain, a sulfonylamino group, and a phenoxy group. These groups enable the compound to interact with a broad spectrum of molecules, facilitating diverse chemical reactions. The presence of the trifluoromethanesulfonic acid component further enhances the compound's acidity and reactivity, making it a versatile tool for synthesizing new materials and compounds in research and industrial settings.

1334686-05-3

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1334686-05-3 Usage

Uses

Used in Organic Synthesis:
Trifluoromethanesulfonic acid 4-(2-tert-butoxyethoxy)-6-(4-tert-butylbenzenesulfonylamino)-5-(2-methoxyphenoxy)pyrimidin-2-yl ester is used as a reagent for its strong acid catalytic properties, which are essential in various organic synthesis reactions. Its ability to interact with a wide range of molecules makes it a valuable component in the synthesis of new materials and compounds.
Used in Research and Development:
In the field of research and development, trifluoromethanesulfonic acid 4-(2-tert-butoxyethoxy)-6-(4-tert-butylbenzenesulfonylamino)-5-(2-methoxyphenoxy)pyrimidin-2-yl ester is employed as a catalyst to facilitate chemical reactions and the synthesis of novel compounds. Its versatility in interacting with different molecular structures allows researchers to explore new avenues in chemical synthesis and material development.
Used in Pharmaceutical Industry:
Trifluoromethanesulfonic acid 4-(2-tert-butoxyethoxy)-6-(4-tert-butylbenzenesulfonylamino)-5-(2-methoxyphenoxy)pyrimidin-2-yl ester is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique functional groups and reactivity enable the creation of new drug molecules with potential therapeutic applications.
Used in Material Science:
In material science, trifluoromethanesulfonic acid 4-(2-tert-butoxyethoxy)-6-(4-tert-butylbenzenesulfonylamino)-5-(2-methoxyphenoxy)pyrimidin-2-yl ester is utilized as a building block for the development of new materials with specific properties. Its ability to participate in various chemical reactions allows for the creation of materials with tailored characteristics for use in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1334686-05-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,6,8 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1334686-05:
(9*1)+(8*3)+(7*3)+(6*4)+(5*6)+(4*8)+(3*6)+(2*0)+(1*5)=163
163 % 10 = 3
So 1334686-05-3 is a valid CAS Registry Number.

1334686-05-3Downstream Products

1334686-05-3Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF BOSENTAN

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, (2011/10/13)

The present invention provides a novel process for obtaining Bosentan, with few synthesis steps, by coupling the intermediate pyrimidine compound of formula I with the sulfonamide compound of formula II. The use of said efficient process prevents the use of hazardous chemicals and thus it is of considerable interest for obtaining Bosentan in a large industrial scale. The invention also refers to the novel intermediates of formula II and to a process for its production.

Process for the preparation of bosentan

-

, (2011/10/12)

The present invention provides a novel process for obtaining Bosentan, with few synthesis steps, by coupling the intermediate pyrimidine compound of formula I with the sulfonamide compound of formula II. The use of said efficient process prevents the use of hazardous chemicals and thus it is of considerable interest for obtaining Bosentan in a large industrial scale. The invention also refers to the novel intermediates of formula II and to a process for its production.

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