Amino Acids, Proteins and Nucleic Acids
Alcohols, Phenols and Ethers
Organo Silicon Compounds
Halides
Heterocyclic Compounds
Organic Fluorine Compounds
Nitrogen Compounds
Organometallic Compounds
Esters
Hydrocarbons
Aromatic Compounds
Carboxylic Acids and Derivatives
Nitriles
Organometalate
Aldehydes, Ketones and Quinones
Carbohydrate
CAS:99844-02-7
Molecular Formula:C11H11N3O
Alias
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4-(4-Methoxyphenyl)-2-Pyrimidinamine; 2-Amino-4-(4-Methoxyphenyl)Pyrimidine; [4-(4-Methoxyphenyl)Pyrimidin-2-Yl]Amine; 2-Pyrimidinamine, 4-(4-Methoxyphenyl)-
CAS:99931-82-5
Molecular Formula:C8H11BrN4
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5-Bromo-2-Piperazin-1-Yl-Pyrim; (5-Bromopyrimidin-2-Yl)Piperazine; 2-[N-(4-Aminophenyl)Amino]-4,6-Dimethylpyrimidine; 5-Bromo-2-(1-Piperazin-4-Iumyl)Pyrimidine; 1-(5-Bromopyrimidin-2-Yl)Piperazine; 5-Bromo-2-Piperazinopyrimidine
Brief Introduction
An organic intermediate can be prepared from 5-bromo-2-chloropyrimidine and N-methylpiperazine by one-step reaction.
CAS:99960-09-5
Molecular Formula:C10H9NO2S
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2-Isothiocyanato-Benzoic Acid Ethyl Ester; 2-(Etoxycarbonyl)Phenylisothiocyanate; Ethyl 2-Isoithiocyanatobenzoate
CAS:6613-64-5
Molecular Formula:C10H13NO3S
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1-(3-Sulfopropyl)-2-Vinylpyridinium Betaine; 3-(2-Vinylpyridinium-1-Yl)Propane-1-Sulfonate; 3-(2-Vinylpyridin-1-Ium-1-Yl)Propane-1-Sulfonate; 1-(3-Sulfopropyl-1)-2-Vinyl Pyridinium Betaine; 1-(3-Sulfopropyl)-2-Vinyl Pyridinium Betaine; 3-(2-Ethenylpyridin-1-Ium-1-Yl)Propane-1-Sulfonate
Brief Introduction
This product is organic and can be used as polymer synthetic monomer.
CAS:75-44-5
Molecular Formula:CCl2O
Alias
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Phlsgene; Phosgenegas; Fosgen; Carbonic Dichloride; Dichloro-Ketone; Carbonyl Chloride; Combatgas; Phosgen; Thionyl Chloride; Fosgene; Fosgeen
Brief Introduction
Phosgene, viewed from the chemical structure, is a diacyl chloride derivative of carbonic acid. It is a very active electrophilic reagent and easy to hydrolyze. It is a severe asphyxiating toxic gas. Inhalation of high concentration can cause pulmonary edema. The toxicity is about 10 times greater than that of chlorine, but it has no accumulation effect in the body. Its common name is translated from Greek φως (light) + Γίνει (generated). Phosgene was originally produced by the decomposition of chloroform by light, so it has this name.
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