19056-49-6 Usage
Chemical structure
A tetrahydrofuran ring with an iodomethyl group and a methyl group attached to it.
Usage
Commonly used as an intermediate in the synthesis of various organic compounds and pharmaceuticals.
Reactivity
Known for its ability to undergo various reactions, such as nucleophilic substitution and metal-catalyzed processes.
Versatility
Acts as a versatile building block for the production of complex organic molecules.
Potential applications
Studied for its potential use as a reagent in organic chemistry and as a precursor in the creation of functionalized heterocycles.
Hazardous nature
Considered hazardous and may pose health risks if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 19056-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19056-49:
(7*1)+(6*9)+(5*0)+(4*5)+(3*6)+(2*4)+(1*9)=116
116 % 10 = 6
So 19056-49-6 is a valid CAS Registry Number.
19056-49-6Relevant articles and documents
Stereocontrolled Synthesis of Cis-2,5-Disubstituted Tetrahydrofuranes and cis- and trans-Linalyl Oxides
Rychovsky, Scott D.,Bartlett, Paul A.
, p. 3963 - 3964 (1981)
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Iodocyclization of olefinic t-butyl ethers: An easy stereocontrolled synthesis of cis-substituted tetrahydrofurans
Marek,Lefrancois,Normant
, p. 1747 - 1748 (2007/10/02)
The iodoalkoxylation of δ,ε olefinic t-butyl ethers leads, with a very high selectivity, to cis substituted tetrahydrofurans.
STEREOCHEMISTRY OF THE IODOCYCLIZATION OF UNSATURATED ALCOHOLS
Gevaza, Yu. I.,Kupchik, I. P.,Staninets, V. I.
, p. 24 - 26 (2007/10/02)
The corresponding tetrahydrofuran derivatives were obtained by iodination of δ,ε-unsaturated alcohols containing substituents attached to the α-carbon atom.The effect of substituents on the stereochemistry of the products and the rate of iodination of the
