593-66-8 Usage
Description
VINYL IODIDE is a halogenated hydrocarbon compound that consists of a vinyl group (a carbon-carbon double bond) with an iodine atom attached. It is known for its unique chemical properties and reactivity, making it a versatile building block in various chemical and pharmaceutical applications.
Uses
Used in Organic Synthesis:
VINYL IODIDE is used as a key intermediate for the synthesis of various organic compounds. Its presence in the molecule allows for a wide range of reactions, including addition, substitution, and elimination reactions, which can lead to the formation of a diverse array of products.
Used in Chemical Research:
In the field of chemical research, VINYL IODIDE serves as a valuable compound for studying the effects of halogenation on the reactivity and stability of organic molecules. Researchers can use it to explore new reaction pathways and develop innovative synthetic methods.
Used in Pharmaceuticals:
VINYL IODIDE is used as a building block in the development of pharmaceutical compounds. Its unique reactivity allows for the creation of novel drug candidates with potential therapeutic applications. Additionally, its properties can be exploited to design targeted drug delivery systems or to improve the pharmacokinetic and pharmacodynamic properties of existing drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 593-66-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 593-66:
(5*5)+(4*9)+(3*3)+(2*6)+(1*6)=88
88 % 10 = 8
So 593-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H3I/c1-2-3/h2H,1H2
593-66-8Relevant articles and documents
Yamashita et al.
, p. 659,660,662 (1972)
Acyl iodides in organic synthesis: VI. Reactions with vinyl ethers
Voronkov,Trukhina,Vlasova
, p. 467 - 469 (2007/10/03)
Reactions of acetyl iodide with butyl vinyl ether, 1,2-divinyloxyethane, phenyl vinyl ether, 1,4-di-vinyloxybenzene, and divinyl ether were studied. Vinyl ethers derived from aliphatic alcohols (butyl vinyl ether and 1,2-divinyloxyethane) react with acetyl iodide in a way similar to ethyl vinyl ether, i.e., with cleavage of both O-Csp2 and Alk-O ether bonds. From butyl vinyl ether, a mixture of vinyl iodide, butyl acetate, vinyl acetate, and butyl iodide is formed, while 1,2-divinyloxyethane gives rise to vinyl iodide, vinyl acetate, and 2-iodoethyl acetate. The reaction of acetyl iodide with divinyl ether involves cleavage of only one O-Csp2 bond, yielding vinyl acetate and vinyl iodide. In the reactions of acetyl iodide with phenyl vinyl ether and 1,4-divinyloxybenzene, only the O-CVin bond is cleaved, whereas the O-CAr bond remains intact.
Epothilone derivatives and methods for making and using the same
-
, (2008/06/13)
This invention relates to compounds of formula (I) and to pharmaceutically acceptable salts and solvates thereof, wherein R1, R2, R3, R4, R5, W, X, Y, and Ar are as defined herein. Compounds of formula (I) are useful in the treatment of diseases or conditions characterized by cellular hyperproliferation. This invention also relates to means for the preparation of compounds of formula (I); formulations containing compounds of formula (I); and methods for the use of said compounds and formulations in the treatment of a disease or condition characterized by cellular hyperproliferation, including cancer.
