168850-69-9 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4,5-dimethylthiophene-2-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and improve the efficacy of existing ones.
Used in Agrochemical Industry:
Methyl 4,5-dimethylthiophene-2-carboxylate is used as an intermediate in the production of agrochemicals, such as pesticides and herbicides, due to its potential to enhance the effectiveness of these compounds in agricultural applications.
Used in Organic Synthesis:
Methyl 4,5-dimethylthiophene-2-carboxylate is used as a versatile building block in organic synthesis for its ability to be incorporated into a wide range of organic compounds, facilitating the creation of new molecules with various applications.
It is important to handle and store Methyl 4,5-dimethylthiophene-2-carboxylate with care, as it may be hazardous when inhaled, ingested, or comes into contact with skin and eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 168850-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,8,5 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168850-69:
(8*1)+(7*6)+(6*8)+(5*8)+(4*5)+(3*0)+(2*6)+(1*9)=179
179 % 10 = 9
So 168850-69-9 is a valid CAS Registry Number.
168850-69-9Relevant articles and documents
Synthetic Applications of Arenetricarbonylchromium(0) Complexes: the Synthesis of Polyfunctionalised Thiophenes
Loft, Michael S.,Mowlem, Timothy J.,Widdowson, David A.
, p. 97 - 104 (2007/10/02)
Lithiation of thiophenetricarbonylchromium(0) complexes with butyllithium occurs preferentially at C-2/5 but when these are blocked, 3/4 lithiation is facile.Combinations of a bulky silyl (i-Pr3Si or t-BuMe2Si) blocking group at C-2/5 and remote lithiation/electrophilic quench of C-3/4 followed by desilylation/lithiation/electrophilic quench allowed the synthesis of 2,3-, 2,3,5- and 2,3,4,5-polysubstituted thiophene complexes and their derived free thiophenes.