22921-72-8

Basic information

• Product Name: 5-PHENOXYPENTYL BROMIDE
• Synonyms: 1-BROMO-5-PHENOXYPENTANE;5-PHENOXYPENTYL BROMIDE;5-Phenoxyamyl Bromide;5-Phenoxypentyl Bromide 5-Bromoamyl Phenyl Ether 5-Bromopentyl Phenyl Ether
• CAS NO: 22921-72-8
• Molecular Formula: C₁₁H₁₅BrO
• Molecular Weight: 243.14
• Product Categories: Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds
• Mol File: 22921-72-8.mol
• Article Data: 22

Chemical Properties

• Boiling Point: 304.5°Cat760mmHg
• Flash Point: 120.2°C
• Appearance: /
• Density: 1.262g/cm³
• Vapor Pressure: 0.00157mmHg at 25°C
• Refractive Index: 1.526
• CAS DataBase Reference: 5-PHENOXYPENTYL BROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-PHENOXYPENTYL BROMIDE(22921-72-8)
• EPA Substance Registry System: 5-PHENOXYPENTYL BROMIDE(22921-72-8)

Safety Data

• Hazardous Substances Data: 22921-72-8(Hazardous Substances Data)

Usage

General Description

5-PhenoxyPentyl Bromide is a chemical compound with the molecular formula C11H15BrO. It is an alkyl bromide, which is commonly used as a reagent in organic synthesis for the preparation of a wide range of compounds. This chemical is a colorless liquid with a molecular weight of 249.14 g/mol. It is often utilized as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. In addition, it can also be used as a solvent in various chemical processes. 5-PhenoxyPentyl Bromide is known for its mild to moderate toxicity and should be handled with care and proper safety precautions.

InChI:InChI=1/C11H15BrO/c12-9-5-2-6-10-13-11-7-3-1-4-8-11/h1,3-4,7-8H,2,5-6,9-10H2

Upstream product

• 111-24-0 1,5-dibromo-pentane 
• 139-02-6 sodium phenoxide 
• 108-95-2 phenol 
• 2653-86-3 (pent-4-en-1-yloxy)benzene 
• 584-08-7 potassium carbonate 
• 69687-95-2 ethyl 5-(phenoxy)pentanoate 
• 7170-40-3 5-phenoxyvaleric acid 
• 16654-52-7 5-phenoxy-1-pentanol 

Downstream Products

• 16728-57-7 6-phenoxyhexanenitrile 
• 40339-97-7 (5-iodo-pentyl)-phenyl ether 
• 7170-41-4 6-phenoxyhexanoic acid 
• 71933-96-5 dimethyl-(5-phenoxy-pentyl)-amine 
• 53874-02-5 1-[2-Hydroxy-6-(5-phenoxy-pentyloxy)-phenyl]-ethanone 
• 61270-16-4 1-[2-Hydroxy-4-(5-phenoxy-pentylsulfanyl)-phenyl]-ethanone 
• 101719-53-3 1-Phenoxy-5-(4-nitro-2-methoxy-phenoxy)-pentan 
• 51796-00-0 1-Methoxy-2-(6-phenoxy-hexyl)-benzene 
• 126435-91-4 1-phenoxy-7-nonanol 
• 137929-68-1 2-(5-phenoxy-pentyl)-[1,3]dithiane 
• 257290-48-5 2-methyl-8-phenoxy-1-octene 
• 1007863-98-0 1-nitro-3-(5-phenoxypentoxy)benzene 
• 51796-03-3 6-(o-hydroxyphenyl)-1-hexene 
• 1204739-68-3 C₁₆H₂₃NO₂ 

Relevant articles and documents

Self-assembly studies of allosteric photosynthetic antenna model systems

In this paper allosteric interactions are employed to enhance electron transfer in a pseudorotaxane system. Binding of an axial ligand (tbpy) to an electron donating mono-cavity appended zinc porphyrin (ZnP) increases the complexation strength to an elect

2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS

The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.

ω-Phenoxyalkyl substituted bis(indenyl)zirconium dichloride complexes as catalysts for homogeneous ethylene polymerization

Nine bis(indenyl)zirconium dichloride complexes of the type [C9H6-(CH2)n-O-Ar]2ZrCl2 (n = 3-5; Ar = Ph, t-Bu-Ph) were synthesized, characterized, activated with methylalumoxane (MAO) and tested for ethylene polymerization. Structure-property-relationship studies showed that the activities of the catalysts depend on the length of the bridging chain between the indenyl and the phenoxy group as well as on the bulk at the phenoxy substituent. A t-Bu substituent at the ortho position of the phenoxy group (5a/MAO) gives a much higher catalyst activity (27,500 kg PE/mol cat h) than the isomer 8a/MAO with a t-Bu substituent at the para position of the phenoxy group (16,700 kg PE/mol cat h). Obviously substituents in the ortho position of the phenyl ring generate a bulkier catalyst cation and this can keep the MAO anion at a further distance to allow easier ethylene coordination and chain growth in the polymerization steps. The mono substituted bis(indenyl) complex (C9H7)[C9H6-(CH2)4-O-4-t-Bu]ZrCl2 shows lower activity (11,700 kg PE/mol cat h) than 8a indicating that the electronic effect is dominating in this type of catalysts.