5831-70-9 Usage
Uses
Used in Organic Synthesis:
2-(Iodomethyl)tetrahydrofuran is used as a reagent in organic synthesis for its highly reactive alkylating properties, which allow for the formation of various chemical compounds.
Used in Pharmaceutical Industry:
2-(Iodomethyl)tetrahydrofuran is used as an intermediate in the preparation of various pharmaceuticals, contributing to the development of new drugs and treatments.
Used in Agrochemical Industry:
2-(IODOMETHYL)TETRAHYDROFURAN is also utilized in the preparation of agrochemicals, playing a role in the development of pesticides and other agricultural products.
Safety Precautions:
It is important to handle 2-(iodomethyl)tetrahydrofuran with caution due to its toxic nature and potential hazards to human health and the environment. Proper safety precautions and equipment should be used when working with 2-(IODOMETHYL)TETRAHYDROFURAN to avoid harmful effects.
Check Digit Verification of cas no
The CAS Registry Mumber 5831-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5831-70:
(6*5)+(5*8)+(4*3)+(3*1)+(2*7)+(1*0)=99
99 % 10 = 9
So 5831-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H9IO/c6-4-5-2-1-3-7-5/h5H,1-4H2
5831-70-9Relevant academic research and scientific papers
A mild method for generation of p-methoxybenzyl cation through NIS- mediated activation of p-methoxybenzyl 4-pentenyl ether
Okada,Kitagawa,Fujita,Taguchi
, p. 8135 - 8142 (2007/10/03)
A mild and facile method for generation of p-methoxybenzyl cation through NIS-mediated activation of p-methoxybenzyl 4-pentenyl ether was achieved. Under the present activation conditions, various alcohols were convened to the corresponding p-methoxybenzyl ethers. A scope and limitation of the present p-methoxybenzylation reaction was also investigated.
Intramolecular Addition of Alkoxy Radicals. Part 4. Reductive Cyclisation of Olefinic Hydroperoxides
Taillez, Bernard,Bertrand, Michele Paula,Surzur, Jean-Marie
, p. 547 - 554 (2007/10/02)
Pent-4-enyl hydroperoxide reacts with reducing salts (FeX2, TiCl3) to afford tetrahydrofurfuryl compounds (halides or dimers) in high yield from the selective cyclisation of the pent-4-enyloxy radical.Analogous behaviour is observed for photolysis although the yields of cyclic products are lower.The photolysis of hex-5-enyl hydroperoxide does not yield cyclic products but these are observed when this hydroperoxide is reduced by FeCl2.It is suggested that metallic salts are able to complex the alkoxyl radicals thereby making them more electrophilic and hence more prone to cyclise.
