624-66-8 Usage
Uses
Used in Organic Synthesis:
1-Propyn-1-yl iodide is used as a building block for the synthesis of various organic compounds, particularly alkynes and alkenes. Its reactivity and versatility make it a valuable precursor in the preparation of a wide range of chemical products.
Used in Pharmaceutical Industry:
1-Propyn-1-yl iodide is used as a key intermediate in the synthesis of pharmaceutical compounds. Its ability to form stable bonds with other molecules allows for the creation of new drug candidates with potential therapeutic applications.
Used in Chemical Research:
1-Propyn-1-yl iodide is employed in academic and industrial research settings to study the properties and reactions of organoiodine compounds. Its unique chemical structure provides insights into the behavior of similar compounds and contributes to the development of new synthetic methods and strategies.
Used in Material Science:
1-Propyn-1-yl iodide is utilized in the development of new materials with specific properties, such as conductivity, stability, or reactivity. Its incorporation into polymers or other materials can lead to the creation of advanced materials with applications in various industries, including electronics, energy, and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 624-66-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 624-66:
(5*6)+(4*2)+(3*4)+(2*6)+(1*6)=68
68 % 10 = 8
So 624-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H3I/c1-2-3-4/h1H3
624-66-8Relevant academic research and scientific papers
Wu, Boshen,Feast, George C.,Thompson, Amber L.,Robertson, Jeremy
, p. 10623 - 10630 (2012)
An 11-step synthesis is described of two diastereomeric candidates for a bis(acetylenic) enol ether spiroacetal isolated from Chrysanthemum boreale. Key steps in the synthetic route include spiroacetal lactone alkylidenation and subseqent modified Cadiota-Chodkiewicz cross-coupling to install the bis(acetylenic) enol ether functionality. From NMR comparisons, neither of the candidates, whose structures were confirmed by single-crystal X-ray diffraction, correspond to the natural product, and a proposal for the correct structure is put forward.
A short and efficient synthesis of the polyacetylene natural product deca-4,6,8-triyn-1-ol
Machado, Vanessa Rocha,Biavatti, Maique Weber,Danheiser, Rick L.
, p. 3405 - 3408 (2018/08/21)
A practical and efficient four-step synthesis of the natural product deca-4,6,8-triyn-1-ol has been achieved beginning with (triisopropylsilyl)acetylene. This trialkyne has potential utility as a key intermediate for the total synthesis of the antitumor butenolide natural product vernoniyne.
