Flexible application of in synthetic route 616-14-8

In some applications, this compound(616-14-8)Application In Synthesis of 1-Iodo-2-methylbutane is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 1-Iodo-2-methylbutane(SMILESS: CCC(CI)C,cas:616-14-8) is researched.SDS of cas: 1968-05-4. The article 《Kinetics, products and mechanism of O(3P) atom reactions with alkyl iodides》 in relation to this compound, is published in NATO Science Series, IV: Earth and Environmental Sciences. Let’s take a look at the latest research on this compound (cas:616-14-8).

Alkyl halides are an important source of halogens in the atm. In the case of alkyl iodides, relative kinetic studies of their OH reactions in photoreactors are complicated by fast reactions with the O(3P) atoms generated by the photochem. OH radical sources. In the present study, the relative kinetic technique was applied in large and small photoreactors to measure rate coefficients for the reaction of O(3P) atoms with a series of alkyl iodides at room temperature and atm. pressure. The products formed in N2 were also investigated. Alkenes and HOI are the major products of the reactions and the alkene was quantified for the majority of the alkyl iodides studied.

In some applications, this compound(616-14-8)Application In Synthesis of 1-Iodo-2-methylbutane is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Thiomorpholine – Wikipedia,
Thiomorpholine | C4H9NS – PubChem