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Methyl 3-((trimethylsilyl)ethynyl)picolinate is a chemical compound that is a derivative of picolinic acid, featuring a trimethylsilyl group and an ethynyl group. It is known for its versatile reactivity and ability to react with a wide range of substrates, making it a valuable tool in organic synthesis and as a reagent in chemical reactions.

219623-03-7

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219623-03-7 Usage

Uses

Used in Organic Synthesis:
Methyl 3-((trimethylsilyl)ethynyl)picolinate is used as a reagent in organic synthesis for the preparation of various functionalized molecules. Its versatile reactivity allows it to be employed in a wide range of chemical reactions, contributing to the synthesis of complex organic compounds.
Used in Material Science:
In the field of material science, methyl 3-((trimethylsilyl)ethynyl)picolinate is used as a precursor in the development of new materials with specific properties. Its unique structure and reactivity enable the creation of materials with potential applications in various industries.
Used in Pharmaceutical Research:
Methyl 3-((trimethylsilyl)ethynyl)picolinate is also utilized in pharmaceutical research for the synthesis of bioactive compounds and drug candidates. Its ability to react with various substrates makes it a promising tool for the development of new pharmaceutical agents with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 219623-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,6,2 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 219623-03:
(8*2)+(7*1)+(6*9)+(5*6)+(4*2)+(3*3)+(2*0)+(1*3)=127
127 % 10 = 7
So 219623-03-7 is a valid CAS Registry Number.

219623-03-7Downstream Products

219623-03-7Relevant articles and documents

Synthesis of heterocyclic dipeptide analogues

Falck-Pedersen, Mette Lene,Undheim, Kjell

, p. 1327 - 1332 (2007/10/03)

Synthesis of constrained mimics of a serine dipeptide is described. Triflated 3-hydroxypicolinic acid methyl ester was carbo-substituted using ethynylstannanes with Pd-catalysis to furnish 3-acetylenic pyridines which were hydrolysed and coupled to Ser(t-Bu)OMe before cyclization to 1-alkylidene-3-oxo-1,3-dihydro-pyrrolo[3,4-b]pyridine derivatives. Subsequent deprotection provided the dipeptide analogue. Acta Chemica Scandinavica 1998.

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