Anthraquinones are a class of aromatic organic compounds having a six-carbon cyclic diketone structure containing two double bonds. For example, p-benzoquinone, o-benzoquinone. Terpenes have the properties of open-chain diketones, which can undergo addition reactions and reduction reactions, and lack the properties of aromatic compounds. The structure and color of the 醌 type are closely related, so most of the quinone compounds are colored substances. Terpenoids also include naphthoquinones, phenanthrenequinones and anthraquinones in a broad sense. Terpenoids are a class of compounds that include steroids or are easily converted to steroids, and are closely related to steroids in biosynthesis. They are often found in nature as pigments in animals, plants, and microorganisms. Many important Chinese medicines such as rhubarb, cassia seed, senna, comfrey, Polygonum cuspidatum, Polygonum multiflorum, aloe vera and other major active ingredients contain terpenoids. According to the chemical structure, terpenoids can be classified into benzoquinones, naphthoquinones, anthraquinones and phenanthrenequinones. Some of these terpenoids play a role in the transfer of electrons in the redox reaction in the body, while others have antibacterial or antitumor activities, such as walnut, sassafras, rapa, etc., and some are the main active ingredients in Chinese herbal medicine. For example, shikonin and isotonicin which have hemostasis, anti-inflammatory, anti-viral and anti-tumor activities in comfrey are the main active ingredients of comfrey. When a quinone compound has no phenolic hydroxyl group in the molecule, it is almost colorless. With the introduction of a chromophore such as a phenolic hydroxyl group, the color of the chromophore is more. The more the chromophore is introduced, the deeper the color, the yellow, orange, Brown red, purple red, etc. Most of the anthraquinone derivatives are yellow to orange red. Most of the natural terpenoids are colored crystals, and benzoquinones and naphthoquinones are mostly present in free state, while terpenoids are often combined with strontium and exist in traditional Chinese medicines, and most of them are difficult to obtain good crystallization. Free hydrazine and hydrazine derivatives have sublimation properties. Small molecules of phenylhydrazine and naphthoquinones are volatile and can be distilled with steam. The free hydrazine and hydrazine derivatives are soluble in organic solvents such as methanol, ethanol, ethyl acetate, diethyl ether, benzene, chloroform, etc., and are sparingly soluble or insoluble in water. It is soluble in methanol and ethanol after being combined with strontium. It is soluble in hot water, but it has low solubility in cold water and is almost insoluble in non-polar organic solvents such as benzene, ether and chloroform.
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Amino compound
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Oxy-containing amino compound
Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts thereof
Acyclic monoamines, polyamines and their derivatives and salts
Amide compound
Sulfonic acid amino compound
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Alcohols, phenols, phenolic compounds and derivatives
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2-cycloalcohol
Halogenated, sulfonated, nitrated or nitrosated derivatives of alcohols
Extremely halogenated, sulfonated, nitrated or nitrosated derivatives of phenols
Phenol and its halogenated, sulfonated, nitrated or nitrosated derivatives
Acyclic alcohol
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Nitrogen-containing compound
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Nitrile compound
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Organic derivative of hydrazine or hydrazine
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Terpenoid
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Ether compounds and their derivatives
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Ether, ether alcohol
Halogenation, sulfonation, nitration or nitrosation of ethers, ether alcohols, ether phenols
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Aldehyde
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Carboxylic compounds and derivatives
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Cyclic carboxylic acid
Halogenation, sulfonation, nitration or nitrosation of carboxylic acids
Halogenation, sulfonation, nitration or nitration of carboxylic anhydrides
Carboxylic acid halide
Carboxylic esters and their derivatives
Salt of carboxylic acid ester and its derivatives
Acyclic carboxylic acid
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Hydrocarbon compounds and their derivatives
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Aromatic hydrocarbon
Cyclic hydrocarbon
Hydrocarbon sulfonate
Hydrocarbon halide
Hydrocarbon nitrite
Acyclic hydrocarbon
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Ketone compound
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Alkyl ureas and their derivatives and salts
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Inorganic acid ester
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Heterocyclic compound
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Diazo, azo or azo compound
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Organosilicon compound
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Organometallic compound
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Organic palladium
Organic germanium, cobalt, strontium, barium, gallium, germanium, germanium, germanium, germanium, etc.
Organic calcium
Zirconium
Organic potassium
Organic
Organic lithium
Organic
Organic aluminum
Organotin
Organic manganese
Organic sodium
Organic nickel
Organic titanium
Organic iron
Organic copper
Organotin
Organic zinc
Organic
Organic
Organic germanium, mercury, silver, platinum, etc.
Organic germanium, antimony, bismuth, tungsten, antimony, bismuth, lead, vanadium, molybdenum, chromium, antimony, etc.
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Organic sulfur compound
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Organic phosphine compound
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Organometallic salt
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Organic fluorine compound
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Fluorobenzoic acid series
Fluorobenzonitrile series
Fluorobenzaldehyde series
Fluorobenzyl alcohol series
Fluoroanisole series
Fluoroaniline series
Fluorophenylacetic acid series
Fluorophenol series
Fluorobenzoic acid series
Fluoronitrobenzene series
Fluoropyridine series
Potassium fluoroborate series
Fluorobenzyl alcohol series
Fluorotoluene series
Fluorine red series
Fluoroethane series
Fluoropropane series