14414-32-5 Usage
Description
4-Hydroxy-3,5-dimethoxybenzaldehyde azine is a green to yellow fine crystalline powder with unique chemical properties. It is a compound that has been utilized in various applications due to its specific characteristics.
Uses
Used in Enzyme Activity Determination:
4-Hydroxy-3,5-dimethoxybenzaldehyde azine is used as a substrate for determining the enzymatic activity of cuticular laccase and recombinant laccase. It serves as a valuable tool in the study and analysis of these enzymes, contributing to the understanding of their functions and potential applications in various fields.
Different applications in different industries may include its use as an intermediate in the synthesis of pharmaceuticals, dyes, or other specialty chemicals, given its unique chemical structure and properties.
Biochem/physiol Actions
Syringaldazine is a dimer of two molecules of 2,6-dimethoxyphenol linked by an azide bridge. It is a phenolic non-autooxidizable laccase-specific compound, that facilitates the detection of fungal laccase in some varieties of fungi. In addition, it also acts as an indicator for peroxidase activity in fungi.
Check Digit Verification of cas no
The CAS Registry Mumber 14414-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,1 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14414-32:
(7*1)+(6*4)+(5*4)+(4*1)+(3*4)+(2*3)+(1*2)=75
75 % 10 = 5
So 14414-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O6/c1-23-13-5-11(6-14(24-2)17(13)21)9-19-20-10-12-7-15(25-3)18(22)16(8-12)26-4/h5-10,21-22H,1-4H3/b19-9+,20-10+
14414-32-5Relevant articles and documents
Synthesis of azines in solid state: Reactivity of solid hydrazine with aldehydes and ketones
Lee, Byeongno,Hyung Lee, Kyu,Cho, Jaeheung,Nam, Wonwoo,Hur, Nam Hwi
, p. 6386 - 6389 (2011)
Highly conjugated azines were prepared by solid state grinding of solid hydrazine and carbonyl compounds such as aldehydes and ketones, using a mortar and a pestle. Complete conversion to the azine product is generally achieved at room temperature within 24 h, without using solvents or additives. The solid-state reactions afford azines as the sole products with greater than 97% yield, producing only water and carbon dioxide as waste.
Syringaldehyde as a scaffold for the synthesis of some biologically potent heterocycles
Azab, Mohammad E.,Elsayed, Galal A.,Emara, Samir A.,Hemdan, Magdy M.,Kamel, Rabaa M.,Youssef, Ahmed S. A.
, (2020/02/13)
Syringaldehyde was utilized in synthesis of different heterocyclic systems. Some of the synthesized compounds 2, 7, 8, 10, 11, and 13 were tested for antioxidant activity where they showed ability to inhibit oxidation in kidney and rat brain homogenates using 2, 2′-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). Also, the activity against cancer was examined using the standard MTT method for two human tumor cell lines namely; mammary gland breast cancer MCF-7 and hepatocellular carcinoma HepG2. The highest activity as antioxidant and antitumor agents was exhibited by compounds 8 and 11. However, moderate activities were shown by compounds 10 and 13. While, compounds 2, 7 showed weak activities.
