Brief introduction of 2689-65-8

In some applications, this compound(2689-65-8)Product Details of 2689-65-8 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Furan derivatives. LV. Kinetics of condensation of 5-nitrofurfuryl sulfones with aldehydes, published in 1975, which mentions a compound: 2689-65-8, mainly applied to kinetics condensation aldehyde nitrofurfuryl sulfone; substituent effect condensation aldehyde nitrofurfuryl sulfone; reaction constant condensation aldehyde nitrofurfuryl sulfone; furfuryl sulfone condensation aldehyde nitrofurfuryl sulfone, Product Details of 2689-65-8.

The kinetics of the condensation of I with II (R = H, Me, iodo, Cl, Br, CO2Me NO2) or III (R = H, NO2, Cl, Br, CO2H, CO2Et, Me, MeO, NHAc) [to give, resp., the corresponding (E)-IV or (E)-V, examined in NH4OAc-piperidine at 118° or MeOH-piperidine at 40°, were 2nd order. The log k was linearly related with σp+. The pKa of I and of 5-nitrofurfuryl Me sulfone (VI) were determined and the rates of the condensation of I or VI with III (R = NO2) indicated that steric factors were more important in the condensation than was the sulfone acidity.

In some applications, this compound(2689-65-8)Product Details of 2689-65-8 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem