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:300-57-2
Molecular Formula:C9H10
Alias
More Information
2-Propenylbenzene; Benzene,Allyl; 3-Phenyl-1-Propene; Allyl-Benzene; 1-Propene,3-Phenyl; Benzene,2-Propenyl; Benzene, 2-Propenyl-; 3-Phenylpropene; Phenylenemethyl-Ethylene; Allylbenzene; 1-Benzylethene; 1-Benzylethylene; 1-Phenyl-2-Propene; 1-Allylbenzene; 1-Propene,3-Phenyl-
Brief Introduction
2-Propenylbenzene, is the primary constituents of various essential oils. It is also an organic building block used for the preparation of various chemicals. It can be used for the production of structurally diverse α,β-unsaturated esters via oxidative alkoxycarbonylation with carbazates.
CAS:3739-67-1
Molecular Formula:C21H24O2
Alias
More Information
bis(alyl Ether) of 4,4'-Isopropylidene Diphenol; Benzene,1,1'-(1-Methylethylidene)bis(4-(2-Propenyloxy); Bisphenol A Diallyl Ether; BBE; 4,4'-Isopropylidenebis[(Allyloxy)Benzene]; bis(Allyl Ether) of 4,4'-Isopropylidenediphenol; 2,2-bis-(4-Allyloxy-Phenyl)-Propane; 2,2-Bis-(4-Allyloxy-Phenyl)-Propan
Brief Introduction
Bisphenol A diallyl ether is an important intermediate in organic synthesis, which is mainly used as crosslinking agent of epoxy resin. At present, most of the methods to synthesize bisphenol A diallyl ether are to add bisphenol A and base into the solvent to form bisphenol a salt, and then add allyl halide to etherify the product. This requires the use of additional solvents. The recovery and treatment of solvents not only increases the cost, but also most of the solvents used are harmful to the environment. The prior art uses ethanol as the solvent and bisphenol A, sodium hydroxide and chloropropene as raw materials to synthesize bisphenol A diallyl ether. This method uses ethanol as solvent. Although it is relatively environmentally friendly, it is difficult to reuse ethanol due to the production of water in the reaction, and excess chloropropene will react with ethanol to produce chloropropene ether. The product synthesized by this method has deep color and needs to be washed with toluene and adsorbed with activated carbon to obtain qualified products, which virtually increases the use of solvent. In the prior art, toluene and diallyl ether are used as solvents to react allyl alcohol with bisphenol A under catalyst conditions to obtain bisphenol A diallyl ether. This method will produce many by-products and the yield is very low.
CAS:378746-64-6
Molecular Formula:C20H25N3O4
Alias
More Information
3-Quinolinecarboxylic Acid, 7-[(3S,5S)-3-Amino-5-Methyl-1-Piperidinyl]-1-Cyclopropyl-1,4-Dihydro-8-Methoxy-4-Oxo-; 7-[(3S,5S)-3-Amino-5-Methyl-1-Piperidinyl]-1-Cyclopropyl-1,4-Dihydro-8-Methoxy-4-Oxo-3-Quinolinecarboxylic Acid; 7-[(3S,5S)-3-Amino-5-Methylpiperidin-1-Yl]-1-Cyclopropyl-8-Methoxy-4-Oxoquinoline-3-Carboxylic Acid
CAS:40925-68-6
Molecular Formula:C6H6BrNO
Alias
More Information
5-Bromo-2-Hydroxyaniline; 2-Amino-4-Bromo-Phenol; 4-Bromo-2-Aminophenol
CAS:41481-63-4
Molecular Formula:C18H18O4S
Alias
More Information
4-Alloxyphenyl Sulfone; 4,4'-Diallyloxydiphenylsulfon; 1,1'-Sulfonylbis[4-(2-Propenyl)OXY-Benzene]; 1-Prop-2-Enoxy-4-(4-prop-2-Enoxyphenyl)Sulfonyl-Benzene; 4,4'-Diallyloxydiphenyl Sulfone; BIS(4-Allyloxyphenyl)Sulfone; 1,1'-Sulfonylbis[4-(prop-2-en-1-Yloxy)Benzol]
Brief Introduction
Used as a research compound.
Inquiry (
10
/ 10
)
Clear All
Sign In
Error!