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5386-25-4

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5386-25-4 Usage

Description

2-Hydroxy-1-naphthoic aldehyde, also known as salicylaldehyde, is a chemical compound that features a naphthalene ring with a hydroxyl group and an aldehyde functional group. It is widely recognized for its role as a building block in the synthesis of various organic compounds and as a precursor in the production of pharmaceuticals, fragrances, and dyes. Its fluorescent properties make it a valuable fluorescent probe in biological and chemical research, and its ability to form stable metal complexes contributes to its applications in coordination chemistry. This versatile chemical compound is utilized across a range of industries and research fields.

Uses

Used in Pharmaceutical Industry:
2-Hydroxy-1-naphthoic aldehyde is used as a precursor for the synthesis of various pharmaceuticals due to its reactive functional groups, which allow for the creation of a wide array of medicinal compounds.
Used in Fragrance Industry:
In the fragrance industry, 2-hydroxy-1-naphthoic aldehyde is used as a building block for creating different types of scents, capitalizing on its ability to form complex and diverse organic compounds.
Used in Dye Industry:
2-Hydroxy-1-naphthoic aldehyde is utilized as a precursor in the production of dyes, where its chemical structure contributes to the development of a variety of colorants.
Used in Research as a Fluorescent Probe:
2-Hydroxy-1-naphthoic aldehyde is employed as a fluorescent probe in biological and chemical research, taking advantage of its fluorescent properties to track and visualize specific processes or substances.
Used in Coordination Chemistry:
In the field of coordination chemistry, 2-hydroxy-1-naphthoic aldehyde is used for forming stable metal complexes, which have potential applications in various areas such as catalysis and material science.

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

5386-25-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-HYDROXY-1-NAPHTHALDEHYDE

1.2 Other means of identification

Product number -
Other names 1-Hydroxymethyl-naphthol-(2)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5386-25-4 SDS

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

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