(2-Bromoethyl)benzene
CAS number: 103-63-9
MSDS Link: Click here
Groups: All Chemicals
Information:
IUPAC Name: 2-bromoethylbenzene
CAS Number: 31620-80-1
Chemical Formula: C8H9Br
Synonyms: 103-63-9, 1-Bromo-2-phenylethane, 2-bromoethylbenzene, 2-bromoethyl-benzene, (2-BROMOETHYL)BENZENE, 2-(BROMOETHYL)BENZENE, (2-Bromoethyl)polystyrene, 2-Phenethyl bromide, 2-Phenyl-1-bromoethane, 2-Phenylethyl bromide, 31620-80-1, 81535_FLUKA, AI3-11264, ar-Monobromoethylbenzene, B65780_ALDRICH, Benzene, (2-bromoethyl)-, Benzene, bromoethyl-, .beta.-Bromoethylbenzene, beta-Bromoethylbenzene, .beta.-Phenethyl bromide, .beta.-Phenylethyl bromide, Bromoethylbenzene, C8H9Br, CID7666, EINECS 203-130-8, EINECS 250-734-2, HSDB 5352, LS-29200, MLS001055470, NCGC00090999-01, NSC33926, NSC 33926, NSC 6534, Phenethyl bromide, Phenylethyl bromide, Phenylethyl bromide (VAN), Polystyrene A-Br, SMR001227201
Product Info: Halogenoalkanes, also known as haloalkanes or alkyl halides, are organic compounds in which one or more hydrogen atoms in an alkane have been replaced by halogen atoms, fluorine, chlorine, bromine or iodine. In carbon-halogen bond, halogens have significantly greater electronegativities than carbon except iodine. In result, this functional group is polarized so that the carbon is electrophilic and the halogen is nucleophilic. Halogenoalkanes are can be classified depending on the halogen atom position on the chain of carbon atoms. The carbon which is attached with the halogen atom is linked up with only one other alkyl group in primary halogenoalkanes, whereas directly linked up with two and three other alkyl groups in secondary halogenoalkanes and tertiary halogenoalkanes respectively. In some case, primary halogenoalkanes are counted even though there are no alkyl groups attached to the carbon with the halogen on it. Three characteristics provide important influences on the chemical behavior of halogenoalkanes, these are electronegativity, covalent bond strength and the relative stability of the corresponding halide anions. Fluoroalkanes have the strongest of the carbon-halogen covalent bonds so that they are unreactive. This is stronger single bond than a carbon-carbon bond. The carbon-chlorine covalent bond is slightly weaker than a carbon-carbon bond, and the bonds to the other halogens are weaker. The stability may be estimated from the relative acidities of the H-X acids. All the hydrohalic acids are very strong, but with small differences in the direction HCl < HBr < HI, with the exception of HF. Halogenoarenes, also called haloarene, or aryl Halide, are an organic compound in which one or more hydrogen atoms in an aromatic ring have been replaced by halogen atoms. The Haloarenes exhibit many differences compare to haloalkanes in the method of preparation and their chemical and phisical properties. Haloalkanes are used in as refrigerants, solvents, blowing agents, aerosol propellants, fire extinguishing media , and in semiconductor device fabrication. One of big consumption of halogenoalkanes (properly speaking, halogenoalkenes) is as a raw material to prepare plastics such as PVC [poly(chloroethene)] from chloroethene and PTFE [poly(tetrafluoroethene)] from tetrafluoroethene. Halogenoalkanes and halogenoarenes react with lots of compounds resulting in a wide range of different target substances. They are useful intermediates in making other organic compounds.
(Both protic and aprotic polar solvent enhance SN1 due to the stabilization of the carbocation intermediate)
* Leaving group Among halogens: I > Br > Cl > F
1-Bromododecane, fatty bromide, is used as a solvent. It is used as an intermediate to manufacture surfactant, pharmaceuticals and other organic compounds.
ASK FOR QUOTATIONMSDS Link: Click here
Groups: All Chemicals
Information:
IUPAC Name: 2-bromoethylbenzene
CAS Number: 31620-80-1
Chemical Formula: C8H9Br
Synonyms: 103-63-9, 1-Bromo-2-phenylethane, 2-bromoethylbenzene, 2-bromoethyl-benzene, (2-BROMOETHYL)BENZENE, 2-(BROMOETHYL)BENZENE, (2-Bromoethyl)polystyrene, 2-Phenethyl bromide, 2-Phenyl-1-bromoethane, 2-Phenylethyl bromide, 31620-80-1, 81535_FLUKA, AI3-11264, ar-Monobromoethylbenzene, B65780_ALDRICH, Benzene, (2-bromoethyl)-, Benzene, bromoethyl-, .beta.-Bromoethylbenzene, beta-Bromoethylbenzene, .beta.-Phenethyl bromide, .beta.-Phenylethyl bromide, Bromoethylbenzene, C8H9Br, CID7666, EINECS 203-130-8, EINECS 250-734-2, HSDB 5352, LS-29200, MLS001055470, NCGC00090999-01, NSC33926, NSC 33926, NSC 6534, Phenethyl bromide, Phenylethyl bromide, Phenylethyl bromide (VAN), Polystyrene A-Br, SMR001227201
Product Info: Halogenoalkanes, also known as haloalkanes or alkyl halides, are organic compounds in which one or more hydrogen atoms in an alkane have been replaced by halogen atoms, fluorine, chlorine, bromine or iodine. In carbon-halogen bond, halogens have significantly greater electronegativities than carbon except iodine. In result, this functional group is polarized so that the carbon is electrophilic and the halogen is nucleophilic. Halogenoalkanes are can be classified depending on the halogen atom position on the chain of carbon atoms. The carbon which is attached with the halogen atom is linked up with only one other alkyl group in primary halogenoalkanes, whereas directly linked up with two and three other alkyl groups in secondary halogenoalkanes and tertiary halogenoalkanes respectively. In some case, primary halogenoalkanes are counted even though there are no alkyl groups attached to the carbon with the halogen on it. Three characteristics provide important influences on the chemical behavior of halogenoalkanes, these are electronegativity, covalent bond strength and the relative stability of the corresponding halide anions. Fluoroalkanes have the strongest of the carbon-halogen covalent bonds so that they are unreactive. This is stronger single bond than a carbon-carbon bond. The carbon-chlorine covalent bond is slightly weaker than a carbon-carbon bond, and the bonds to the other halogens are weaker. The stability may be estimated from the relative acidities of the H-X acids. All the hydrohalic acids are very strong, but with small differences in the direction HCl < HBr < HI, with the exception of HF. Halogenoarenes, also called haloarene, or aryl Halide, are an organic compound in which one or more hydrogen atoms in an aromatic ring have been replaced by halogen atoms. The Haloarenes exhibit many differences compare to haloalkanes in the method of preparation and their chemical and phisical properties. Haloalkanes are used in as refrigerants, solvents, blowing agents, aerosol propellants, fire extinguishing media , and in semiconductor device fabrication. One of big consumption of halogenoalkanes (properly speaking, halogenoalkenes) is as a raw material to prepare plastics such as PVC [poly(chloroethene)] from chloroethene and PTFE [poly(tetrafluoroethene)] from tetrafluoroethene. Halogenoalkanes and halogenoarenes react with lots of compounds resulting in a wide range of different target substances. They are useful intermediates in making other organic compounds.
(Both protic and aprotic polar solvent enhance SN1 due to the stabilization of the carbocation intermediate)
* Leaving group Among halogens: I > Br > Cl > F
1-Bromododecane, fatty bromide, is used as a solvent. It is used as an intermediate to manufacture surfactant, pharmaceuticals and other organic compounds.
Leave some information and we will contact you ASAP about the quotation of this product!
