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2,3-dihydroxy-4-methylbenzaldehyde, also known as syringaldehyde, is an organic compound with the chemical formula C8H8O3. It is a pale yellow crystalline solid that is soluble in water, ethanol, and ether. 2,3-dihydroxy-4-methylbenzaldehyde is derived from the natural compound syringic acid and is an important intermediate in the synthesis of various pharmaceuticals, fragrances, and other organic compounds. Syringaldehyde is characterized by its distinct almond-like odor and is used as a flavoring agent in food and beverages. It is also a key component in the production of vanillin, a widely used artificial vanilla flavoring. The compound can be synthesized through various chemical reactions, including the oxidation of syringol or the condensation of vanillin with acetaldehyde. Due to its versatile applications and natural origin, 2,3-dihydroxy-4-methylbenzaldehyde holds significant value in the chemical and food industries.

6053-03-8

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6053-03-8 Usage

Derivative of benzaldehyde

2,3-dihydroxy-4-methylbenzaldehyde is derived from benzaldehyde, which is a simple aromatic aldehyde.

Hydroxyl and methyl groups

The compound contains two hydroxyl (-OH) groups and a methyl (-CH3) group on the benzene ring, which contribute to its chemical properties and reactivity.

White to pale yellow crystalline appearance

2,3-dihydroxy-4-methylbenzaldehyde forms white to pale yellow crystals, which is a characteristic of its physical appearance.

Synthesis of pharmaceuticals and fine chemicals

2,3-dihydroxy-4-methylbenzaldehyde is commonly used as an intermediate in the synthesis of various pharmaceuticals and fine chemicals due to its reactive functional groups.

Antioxidant and antimicrobial properties

2,3-dihydroxy-4-methylbenzaldehyde has been studied for its potential antioxidant and antimicrobial properties, which could make it useful in various applications, such as food preservation and healthcare.

Inhibition of cancer cell growth

Research has been conducted on the potential of 2,3-dihydroxy-4-methylbenzaldehyde to inhibit the growth of cancer cells, suggesting possible applications in cancer treatment or prevention.

Diverse range of potential applications

The compound has a broad spectrum of potential applications in various fields, including medicine, biotechnology, and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 6053-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6053-03:
(6*6)+(5*0)+(4*5)+(3*3)+(2*0)+(1*3)=68
68 % 10 = 8
So 6053-03-8 is a valid CAS Registry Number.

6053-03-8Downstream Products

6053-03-8Relevant academic research and scientific papers

BORON-CONTAINING SMALL MOLECULES

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Page/Page column 102; 103, (2012/03/27)

This invention relates to, among other items, benzoxaborole compounds and their use for treating bacterial infections.

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