Computed Properties of C7H5BrOIn 2019 ,《Tandem Knoevenagel-Michael-cyclocondensation reaction of malononitrile, various aldehydes and barbituric acid derivatives using isonicotinic acid as an efficient catalyst》 appeared in Progress in Chemical and Biochemical Research. The author of the article were Moosavi-Zare, Ahmad Reza; Goudarziafshar, Hamid; Jalilian, Zahra. The article conveys some information:
Preparation of pyrano[2,3-d]pyrimidine dione derivatives I (R = H, Me; R1 = C6H5, 4-BrC6H4, 2,3-(Cl2)C6H3, etc.) by the tandem Knoevenagel-Michaelcyclocondensation reaction of malononitrile, various aldehydes R1CHO and barbituric acid derivatives like barbituric acid and 1,3-dimethylbarbituric acid in the presence of isonicotinic acid as an efficient organocatalyst has been described. After reading the article, we found that the author used o-Bromobenzaldehyde(cas: 6630-33-7Computed Properties of C7H5BrO)
o-Bromobenzaldehyde(cas: 6630-33-7) is used in L-threonine aldolase-catalyzed enantio/diastereoselective aldol reactions.Computed Properties of C7H5BrOIt is also used in L-threonine aldolase-catalyzed enantio and diastereoselective aldol reactions. Further, it reacts with trichloromethane to prepare 1-(2-bromo-phenyl)-2,2,2-trichloro-ethanol.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary