588-93-2

Basic information

• Product Name: 1-Bromo-4-propylbenzene
• Synonyms: P-BROMOPROPYLBENZENE;1-Brom-4-propylbenzol;4-Propyl-1-bromobenzene;benzene,1-bromo-4-propyl-;4-Bromo-N-Pentylbenzene,5PbrC11H13Br;1-BROMO-4-PROPYLBENZENE / 4-BROMOPROPYLBENZENE;1-BROMO-4-PROPYLBENZENE 99%;4-propyl bromobenzene
• CAS NO: 588-93-2
• Molecular Formula: C₉H₁₁Br
• Molecular Weight: 199.09
• Product Categories: Benzene derivates;4-Alkylbromobenzenes (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials;Aryl;C9 to C12;Halogenated Hydrocarbons;Building Blocks;C9 to C12;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks
• Mol File: 588-93-2.mol
• Article Data: 13

Chemical Properties

• Melting Point: -41.4°C
• Boiling Point: 225 °C(lit.)
• Flash Point: 203 °F
• Appearance: Clear colorless to slightly yellow/Liquid
• Density: 1.286 g/mL at 25 °C(lit.)
• Vapor Pressure: 4.7Pa at 25℃
• Refractive Index: n20/D 1.537(lit.)
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility: 2.867mg/L at 20℃
• CAS DataBase Reference: 1-Bromo-4-propylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-4-propylbenzene(588-93-2)
• EPA Substance Registry System: 1-Bromo-4-propylbenzene(588-93-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• WGK Germany: 3
• Hazardous Substances Data: 588-93-2(Hazardous Substances Data)

Usage

Chemical Properties

Clear colorless to slightly yellow liquid

Uses

Intermediates of Liquid Crystals

Flammability and Explosibility

Notclassified

InChI:InChI=1/C9H11Br/c1-2-3-8-4-6-9(10)7-5-8/h4-7H,2-3H2,1H3

Upstream product

• 2294-43-1 1-allyl-4-bromo-benzene 
• 6186-23-8 1-(4-bromophenyl)propan-2-ol 
• 1124-14-7 1-bromo-4-cyclopropylbenzene 
• 106-37-6 1.4-dibromobenzene 
• 106-94-5 propyl bromide 
• 589-87-7 1,4-bromoiodobenzene 
• 108-86-1 bromobenzene 
• 18620-02-5 (4-bromophenyl)magnesium bromide 
• 108-90-7 chlorobenzene 
• 927-77-5 n-propylmagnesium bromide 
• 103-65-1 phenylpropane 
• 10342-83-3 4'-Bromopropiophenone 

Downstream Products

• 586-76-5 4-Bromobenzoic acid 
• 874646-13-6 (3R)-3-methyl-1-(4-propylphenyl)piperazine 
• 620621-30-9 (1-allyl-1H-pyrazol-5-yl)(4-propylphenyl)methanone 
• 469859-77-6 1-(4-n-propylphenyl)-2-trimethylsilylacetylene 
• 247924-46-5 6-(4-propylphenyl)-2-naphthol 
• 3355-08-6 4-Bromo-2-nitro-1-propyl-benzene 
• 247924-47-6 4-propylphenylboric acid 
• 137489-33-9 4-[2-(p-ethoxyphenyl)ethyl]-2,6-difluoro-4'-n-propylbiphenyl 
• 1046146-13-7 (3,5-dimethoxy-phenyl)-(4-propyl-phenyl)-methanol 
• 1409114-79-9 C₁₆H₁₆O₂ 
• 1235409-88-7 6,13-bis(4-propylphenyl)pentacene 
• 1620662-06-7 diethyl 4-propylphenylphosphonate 
• 1122-91-4 4-bromo-benzaldehyde 
• 6186-22-7 4-bromophenyl acetone 

Relevant articles and documents

Photocatalytic C-O Bond Cleavage of Alcohols Using Xanthate Salts

The homolytic cleavage of C-O bonds to afford alkyl radicals is an attractive yet challenging transformation in organic synthesis. Herein we describe a photocatalyzed deoxygenative C-C coupling reaction of xanthate salts, which can be easily prepared from the corresponding alcohols. The key to the success of this strategy is the low oxidation potential of the xanthate salt and the use of an appropriate phosphine to accelerate the desulfurative release of carbonyl sulfide.

Synthesis method of p-bromo-linear alkylbenzene

The invention belongs to the technical field of fine chemical industry, and in particular discloses a clean and efficient synthetic process technology of p-bromo-linear alkylbenzene. Paradibromobenzene and linear chain 1-haloalkane are added into an organic solvent, and reaction is conducted under the action of a catalyst ferric acetylacetonate and an activating agent consisting of zinc halide and magnesium powder to obtain the p-bromo-linear alkylbenzene. A paradibromobenzene single coupling technology is adopted, so production of ortho/meta isomers which are difficult to separate is avoided from the source; a Grignard reagent, which is instable to water and air, or an expensive boric acid reagent intermediate is not used, so that the production cost is reduced; a one-pot reaction technology is adopted, so that operation is simplified and good industrial application value is achieved.

N-aryl thienyl-, furyl-, and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin

Thienyl-, furyl- and pyrrolyl-sulfonamides and methods for modulating or altering the activity of the endothelin family of peptides are provided. In particular, N-(isoxazolyl)thienylsulfonamides, N-(isoxazolyl)furylsulfonamides and N-(isoxazolyl)pyrrolylsulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided.