The invention discloses a
benzothiazole-cyanophenyl compound serving as a hydrazine
fluorescence probe. The
benzothiazole-cyanophenyl compound has a
structural formula as shown in (I); the compound is prepared by performing cyclodehydration with bromobenzaldehyde and 2-amino-4-chloro
thiophenol serving as the raw materials, then performing coupled reaction in order to connect with a bromobenzaldehyde derivate, and finally performing Knoevenagel reaction with
malononitrile. The
benzothiazole-cyanophenyl compound has the advantages that the raw materials are low in price and easy to
gain, the synthetic
route is simple, and the yield is relatively high; rigid structures such as benzothiazole and
phenylacetylene groups are introduced into such a
fluorescence probe, thus high
fluorescence quantum efficiency is realized, and relatively high
thermal stability and dissolubility are brought. The probe adopts the photoinduced charge
transfer mechanism and the conjugate
passivation mechanism, therefore, a response range respect to hydrazine can be expanded; the probe has the characteristics of being fast in response, high in sensitivity and high in selectivity, is suitable for being applied to safety detection of foods as well as safety detection of a laboratory, in particular applied to industrial
wastewater monitor; and the probe has a wide application prospect in environment monitoring, ecological protection,
disease diagnosis, industrial production and
pollution discharge inspection.