5831-70-9 Usage
Description
2-(Iodomethyl)tetrahydrofuran, also known as iodomethyltetrahydrofuran, is a halogenated organic compound with the molecular formula C5H9IO. It is a highly reactive alkylating agent that is commonly used as a reagent in organic synthesis.
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 this compound 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 articles and documents
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.
