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610-04-8

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610-04-8 Usage

Description

3-FORMYLSALICYLIC ACID, 97, also known as 3-formylsalicylic acid, is a hydroxybenzoic acid derivative in which the hydrogen at position 3 of salicylic acid is substituted by a formyl group. It appears as a beige to light brown crystalline powder and is known for its distinct chemical properties.

Uses

Used in Pharmaceutical Industry:
3-FORMYLSALICYLIC ACID, 97 is used as an intermediate compound for the synthesis of various pharmaceuticals and drugs. Its unique chemical structure allows it to be a key component in the development of new medications, particularly those targeting specific health conditions.
Used in Chemical Synthesis:
In the field of organic chemistry, 3-FORMYLSALICYLIC ACID, 97 serves as a valuable building block for the synthesis of a wide range of chemical compounds. Its formyl group at position 3 enables it to participate in various chemical reactions, making it a versatile starting material for creating complex organic molecules.
Used in Research and Development:
3-FORMYLSALICYLIC ACID, 97 is also utilized in research and development settings, where it can be employed to study the properties and reactivity of formyl-substituted aromatic compounds. This knowledge can be applied to the design and development of new chemical processes and materials with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 610-04-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 610-04:
(5*6)+(4*1)+(3*0)+(2*0)+(1*4)=38
38 % 10 = 8
So 610-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O4/c9-4-5-2-1-3-6(7(5)10)8(11)12/h1-4,10H,(H,11,12)

610-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-formylsalicylic acid

1.2 Other means of identification

Product number -
Other names 2-hydroxy-3-carboxybenzaldehyde

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:610-04-8 SDS

610-04-8Relevant articles and documents

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Ismailskii,Bogoslowksii

, (1937)

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A novel sensitive and selective chemosensor for fluorescent detection of Zn2+in cosmetics creams based on a covalent post functionalized Al-MOF

Kamel, Rasha M.,Shahat, Ahmed,Anwar, Zeinab M.,El-Kady, Hamdy A.,Kilany, Esraa M.

, p. 8054 - 8063 (2021/05/21)

A material was fabricated based on the Schiff base reaction to achieve covalent attachment of NH2-MIL-53(Al) and the 3-formylsalicylic acid ligand (3-FSA) for fluorimetric detection of Zn2+ ions based on inhibition and destruction of CN isomerization and ESIPT. The low limit of detection and limit of quantification were calculated at optimum conditions. The selectivity of the 3-FSA sensor was achieved against some interfering ions. The new sensor was applied for the determination of Zn2+ ions in cosmetic cream products and the obtained results were validated through comparison with ICP-OES. The data indicated that the 3-FSA sensor provided a sensitive, selective, fast, direct and efficient determination of Zn2+ ions with good reproducibility and reversibility.

Synthesis and fluorescence properties of benzoxazole-1,4-dihydropyridine dyads achieved by a multicomponent reaction

Affeldt, Ricardo Ferreira,De Amorim Borges, Ant?nio César,Russowsky, Dennis,Severo Rodembusch, Fabiano

, p. 4607 - 4614 (2014/11/07)

Photoactive 2-(2′-hydroxyphenyl)benzoxazole-1,4-dihydropyridine (HBO-DHP) dyads were obtained by a multicomponent one-pot Hantzsch synthesis using a fluorescent aldehyde, a 1,3-dicarbonylic compound and ammonium acetate. The key step in this synthetic methodology was the synthesis of the formyl benzoxazole derivative through a Duff-modified functionalization protocol. UV-Vis absorption and fluorescence emission spectroscopies were also applied to better understand the photophysics of these compounds. The three novel fluorescent compounds were obtained in moderate yields as stable solids with absorption in the UV region and emission in the blue-green region. Preliminary results indicate that after excitation both HBO and DHP fluorophores behave independently in the HBO-DHP structure. the Partner Organisations 2014.

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