C8H8O3
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C8H8O3
The molecular formula C8H8O3 (molar mass: 152.15 g/mol) may refer to: * Anisic acids ** 2-Methoxybenzoic acid, ''o''-Anisic acid (2-methoxybenzoic acid) ** 3-Methoxybenzoic acid, ''m''-Anisic acid (3-methoxybenzoic acid) ** 4-Methoxybenzoic acid, ''p''-Anisic acid (4-methoxybenzoic acid) * 3,4-Dihydroxyphenylacetaldehyde * 2-Hydroxy-4-methoxybenzaldehyde * 2-Hydroxy-5-methoxybenzaldehyde * Hydroxyphenylacetic acid ** 2-Hydroxyphenylacetic acid ** 3-Hydroxyphenylacetic acid ** 4-Hydroxyphenylacetic acid * Isovanillin * Mandelic acid * Methylparaben * Methyl salicylate * Methylsalicylic acids ** 3-Methylsalicylic acid ** 4-Methylsalicylic acid ** 5-Methylsalicylic acid ** 6-Methylsalicylic acid * Tetrahydrophthalic anhydride * Vanillin * ortho-Vanillin, ''o''-Vanillin {{MolFormDisambig ...
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Vanillin
Vanillin is an organic compound with the molecular formula . It is a phenolic aldehyde. Its functional groups include aldehyde, hydroxyl, and ether. It is the primary component of the ethanolic extract of the vanilla bean. Synthetic vanillin is now used more often than natural vanilla extract as a flavoring in foods, beverages, and pharmaceuticals. Vanillin and ethylvanillin are used by the food industry; ethylvanillin is more expensive, but has a stronger note. It differs from vanillin by having an ethoxy group (−O−CH2CH3) instead of a methoxy group (−O−CH3). Natural vanilla extract is a mixture of several hundred different compounds in addition to vanillin. Artificial vanilla flavoring is often a solution of pure vanillin, usually of synthetic origin. Because of the scarcity and expense of natural vanilla extract, synthetic preparation of its predominant component has long been of interest. The first commercial synthesis of vanillin began with the more readily ...
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Methylparaben
Methylparaben (methyl paraben) one of the parabens, is a preservative with the chemical formula . It is the methyl ester of ''p''-hydroxybenzoic acid. Several related esters are known (ethyl-, propyl-, butylparaben). Together they are the most common preservatives in cosmetics and foods. Among their advantages, parabens are inexpensive, colorless, stable, odorless, and readily biodegraded. Natural occurrences Methylparaben serves as a pheromone for a variety of insects and is a component of queen mandibular pheromone. It is a pheromone in wolves produced during estrus associated with the behavior of alpha male wolves preventing other males from mounting females in heat. Uses Methylparaben is an anti-fungal agent often used in a variety of cosmetics and personal-care products. It is also used as a food preservative and has the E number E218. Methylparaben is commonly used as a fungicide in ''Drosophila'' food media at 0.1%. To ''Drosophila'', methylparaben is toxic ...
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4-Methylsalicylic Acid
4-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. Its functional groups include a carboxylic acid and a phenol group. It is one of four isomers of methylsalicylic acid, including the naturally occurring 6-methylsalicylic acid. The compound has few applications. It is produced by carboxylation of sodium para-cresolate: It has been prepared by hydroxylation of 4-methylbenzoic acid. See also * 3-Methylsalicylic acid * 6-Methylsalicylic acid 6-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 6-methylsalicylate. Its functional groups incl ... References Salicylic acids {{phenol-stub ...
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Methyl Salicylate
Methyl salicylate (oil of wintergreen or wintergreen oil) is an organic compound with the formula C8H8O3. It is the methyl ester of salicylic acid. It is a colorless, viscous liquid with a sweet, fruity odor reminiscent of root beer (in which it is used as a flavoring), but often association (psychology), associatively called "minty", as it is an ingredient in mint candies. It is produced by many species of plants, particularly wintergreens. It is also produced synthetically, used as a fragrance and as a flavoring agent. Biosynthesis and occurrence Methyl salicylate was first isolated (from the plant ''Gaultheria procumbens'') in 1843 by the French chemist Auguste André Thomas Cahours (1813–1891), who identified it as an ester of salicylic acid and methanol. The biosynthesis of methyl salicylate arises via the hydroxylation of benzoic acid by a cytochrome P450 followed by reaction with a methyltransferase enzyme. Methyl salicylate as a plant metabolite Many plants produce ...
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Mandelic Acid
Mandelic acid is an aromatic alpha hydroxy acid with the molecular formula C6H5CH(OH)CO2H. It is a white crystalline solid that is soluble in water and polar organic solvents. It is a useful precursor to various drugs. The molecule is chiral. The racemic mixture is known as ''paramandelic acid''. Isolation, synthesis, occurrence Mandelic acid was discovered in 1831 by the German pharmacist Ferdinand Ludwig Winckler (1801–1868) while heating amygdalin, an extract of bitter almonds, with diluted hydrochloric acid. The name is derived from the German "Mandel" for "almond". Mandelic acid is usually prepared by the acid-catalysed hydrolysis of mandelonitrile, which is the cyanohydrin of benzaldehyde. Mandelonitrile can also be prepared by reacting benzaldehyde with sodium bisulfite to give the corresponding adduct, forming mandelonitrile with sodium cyanide, which is then hydrolyzed: : Alternatively, it can be prepared by base hydrolysis of phenylchloroacetic acid as well as dibrom ...
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2-Methoxybenzoic Acid
''o''-Anisic acid is an organic compound with the formula . A colorless solid, it is one of the isomers of anisic acid. The compound has been well studied with respect to intramolecular hydrogen bond In chemistry, a hydrogen bond (H-bond) is a specific type of molecular interaction that exhibits partial covalent character and cannot be described as a purely electrostatic force. It occurs when a hydrogen (H) atom, Covalent bond, covalently b ...ing and as a substrate for various catalystic reactions. References Benzoic acids 2-Methoxyphenyl compounds Salicylyl ethers {{aromatic-stub ...
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Tetrahydrophthalic Anhydride
Tetrahydrophthalic anhydride is an organic compound with the formula C6H8C2O3. The compound exists as two isomers, this article being focused on the more common cis isomer. It is a white solid that is soluble in organic solvents. Preparation and derivatives Tetrahydrophthalic anhydride, the cis isomer, is prepared by the Diels-Alder reaction of butadiene and maleic anhydride Maleic anhydride is an organic compound with the formula . It is the acid anhydride of maleic acid. It is a colorless or white solid with an acrid odor. It is produced industrially on a large scale for applications in coatings and polymers. Str .... Tetrahydrophthalic anhydride is a precursor to other compounds including the dicarboxylic acid tetrahydrophthalic acid as well the tetrahydrophthalimide, which is a precursor to the fungicide Captan. It is also a precursor to 1,2,3,4-butanetetracarboxylic acid.{{cite journal , doi=10.1107/s0567740871002577 , title=The Crystal Structure of Butane-1,2,3,4-te ...
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6-Methylsalicylic Acid
6-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 6-methylsalicylate. Its functional groups include a carboxylic acid and a phenol Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula . It is a white crystalline solid that is volatile and can catch fire. The molecule consists of a phenyl group () ... group. It is one of four isomers of methylsalicylic acid. It occurs naturally, being a biosynthetic precursor to ''m''-cresol. Its decarboxylation is catalyzed by 6-methylsalicylate decarboxylase: :6-methylsalicylate ⇌ ''m''-cresol + CO2 See also * 4-Methylsalicylic acid * 3-Methylsalicylic acid References Salicylic acids {{phenol-stub ...
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5-Methylsalicylic Acid
5-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 5-methylsalicylate Its functional groups include a carboxylic acid and a phenol group. It is one of four isomers of methylsalicylic acid. It can be prepared by hydroxylation of 3-methylbenzoic acid. See also * 3-Methylsalicylic acid * 4-Methylsalicylic acid * 6-Methylsalicylic acid 6-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 6-methylsalicylate. Its functional groups incl ... References Salicylic acids {{phenol-stub ...
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2-Hydroxy-4-methoxybenzaldehyde
2-Hydroxy-4-methoxybenzaldehyde is a chemical compound and an isomer of vanillin. Urolithin M7, one of the urolithins, has also been synthesized from 2-hydroxy-4-methoxybenzaldehyde using the inverse electron-demand Diels–Alder reaction. See also * Vanillin * 2-Hydroxy-5-methoxybenzaldehyde * Isovanillin Isovanillin is a phenolic aldehyde, an organic compound and isomer of vanillin. It is a selective inhibitor of aldehyde oxidase. It is not a substrate of that enzyme, and is metabolized by aldehyde dehydrogenase into isovanillic acid, which cou ... * ortho-Vanillin References Hydroxybenzaldehydes {{phenol-stub ...
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2-Hydroxy-5-methoxybenzaldehyde
2-Hydroxy-5-methoxybenzaldehyde is an organic compound and an isomer of vanillin. Synthesis and reactions The chemical is produced by the Reimer-Tiemann reaction on 4-methoxyphenol with a 79% yield. It reacts with malononitrile to form 2-imino-6-methoxy-2H-1-benzopyran-3-carbonitrile. It can be reduced by sodium borohydride in ethanol to form 2-hydroxy-5-methoxybenzyl alcohol. See also * Vanillin * Isovanillin * ortho-Vanillin * 2-Hydroxy-4-methoxybenzaldehyde 2-Hydroxy-4-methoxybenzaldehyde is a chemical compound and an isomer of vanillin. Urolithin M7, one of the urolithins, has also been synthesized from 2-hydroxy-4-methoxybenzaldehyde using the inverse electron-demand Diels–Alder reaction. See ... References Phenol ethers Hydroxybenzaldehydes {{aromatic-stub ...
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3-Methylsalicylic Acid
3-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 3-methylsalicylate Its functional groups include a carboxylic acid and a phenol group. It is one of four isomers of methylsalicylic acid. It is produced by carboxylation of sodium o-cresolate: : See also * 4-Methylsalicylic acid * 6-Methylsalicylic acid 6-Methylsalicylic acid is an organic compound with the formula CH3C6H3(CO2H)(OH). It is a white solid that is soluble in basic water and in polar organic solvents. At neutral pH, the acid exists as 6-methylsalicylate. Its functional groups incl ... References Salicylic acids {{phenol-stub ...
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