5386-25-4 Usage
General Description
2-Hydroxy-1-naphthaldehyde, also known as salicylaldehyde, is a chemical compound that contains a naphthalene ring with a hydroxyl group and an aldehyde functional group. It is commonly used as a building block in the synthesis of various organic compounds and as a precursor for the production of pharmaceuticals, fragrances, and dyes. It exhibits fluorescent properties and is often used as a fluorescent probe in biological and chemical research. Additionally, 2-hydroxy-1-naphthaldehyde has applications in the field of coordination chemistry due to its ability to form stable metal complexes. Overall, this chemical compound has diverse uses in various industries and research fields.
Check Digit Verification of cas no
The CAS Registry Mumber 5386-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5386-25:
(6*5)+(5*3)+(4*8)+(3*6)+(2*2)+(1*5)=104
104 % 10 = 4
So 5386-25-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H13ClFNO2/c1-21-16-10-12(5-3-7-20)9-15(18)17(16)22-11-13-4-2-6-14(19)8-13/h2-6,8-10H,11H2,1H3
5386-25-4Relevant articles and documents
Simplified synthesis of 1,1′[14C]-methylene-di (2-naphthol). A radiochemical and kinetic approach
Angelini, Giancarlo,Ursini, Ornella,Minetti, Patrizia,Celona, Diana,De Angelis, Francesco
, p. 543 - 556 (2007/10/03)
The synthesis of the 1,1′[14C]-methylene-di-(2-naphthol) 2, as the radiolabeled probe of a possible interaction between the β-amyloid fibrils and the di-naphthol mojety in the Alzheimer's disease, is reported. Very simple radiochemical procedure, starting from [ 14C]paraformaldehyde, produced 8.66 MBq of compound 2 at the specific radioactivity of 1.22 TBq/mol. A mechanistic and kinetic approach allowed the comprehension of the right experimental conditions. The stability of compound 2 in acetonitrile solution was investigated, denoting a significative decomposition process through the transient formation of the 1,2-naphthyne intermediate. Copyright
