19728-41-7 Usage
Description
2-TERT-BUTYLTHIOPHENOL is an organic compound characterized by the presence of a thiophene ring with a tert-butyl group attached to the 2nd position. It is known for its unique chemical properties and reactivity, making it a valuable component in various scientific and industrial applications.
Uses
Used in Proteomics Research:
2-TERT-BUTYLTHIOPHENOL serves as a specialty product in proteomics research, where it aids in the study of proteins and their interactions within biological systems. Its unique chemical structure allows it to be used as a valuable tool for analyzing and identifying proteins, contributing to a better understanding of their functions and roles in various biological processes.
Used in Organic Synthesis:
In the field of organic synthesis, 2-TERT-BUTYLTHIOPHENOL acts as an intermediate, playing a crucial role in the formation of more complex organic molecules. Its reactivity and structural features make it a versatile building block for synthesizing a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
2-TERT-BUTYLTHIOPHENOL is also utilized as an intermediate in the development and production of pharmaceuticals. Its unique properties and reactivity enable the creation of new drug candidates and the improvement of existing medications, ultimately contributing to advancements in healthcare and the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 19728-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19728-41:
(7*1)+(6*9)+(5*7)+(4*2)+(3*8)+(2*4)+(1*1)=137
137 % 10 = 7
So 19728-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H14S/c1-10(2,3)8-6-4-5-7-9(8)11/h4-7,11H,1-3H3
19728-41-7Relevant articles and documents
Method of preparation of organosilyl substituted aromatic or heteroaromatic compounds
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, (2008/06/13)
An improved method of preparing an ortho-, meta- or para-silyl aromatic or heteroaromatic compound represented by the formula STR1 wherein X is oxygen or sulfur, R1 represents the atoms necessary to complete an unsubstituted or substituted arom
