7295-46-7

Basic information

• Product Name: 4-BROMOPENTANOPHENONE
• Synonyms: 4-BROMOPENTANOPHENONE;4-BROMOPHENYLPENTYL KETONE;1-(4-Bromophenyl)-1-hexanone;4-Bromohexanophenone;1-(4-BroMophenyl)hexan-1-one
• CAS NO: 7295-46-7
• Molecular Formula: C₁₂H₁₅BrO
• Molecular Weight: 255.15
• Product Categories: Aromatic Ketones (substituted)
• Mol File: 7295-46-7.mol
• Article Data: 14

Chemical Properties

• Melting Point: 59-60 ºC
• Boiling Point: 322 ºC
• Flash Point: 48 ºC
• Appearance: /
• Density: 1.255
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.527
• CAS DataBase Reference: 4-BROMOPENTANOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMOPENTANOPHENONE(7295-46-7)
• EPA Substance Registry System: 4-BROMOPENTANOPHENONE(7295-46-7)

Safety Data

• Hazardous Substances Data: 7295-46-7(Hazardous Substances Data)

Usage

General Description

4-Bromopentanophenone is a chemical compound with the molecular formula C11H15BrO. It is a ketone derivative of pentanophenone with a bromine atom attached to the 4th carbon of the alkyl chain. 4-BROMOPENTANOPHENONE is commonly used in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceuticals and biologically active compounds. It is also used as a reagent in chemical reactions, especially in the modification of organic molecules. 4-Bromopentanophenone is a versatile compound with potential applications in drug discovery and development due to its structural features and reactivity.

InChI:InChI=1/C12H15BrO/c1-2-3-4-5-12(14)10-6-8-11(13)9-7-10/h6-9H,2-5H2,1H3

Upstream product

• 71434-62-3 (+/-)-p-bromophenyl-1-hexanol 
• 62-53-3 aniline 
• 190649-11-7 1-bromo-4-(hex-1-yn-1-yl)benzene 
• 693-02-7 hex-1-yne 
• 693-25-4 n-pentylmagnesium bromide 
• 1122-91-4 4-bromo-benzaldehyde 
• 108-86-1 bromobenzene 
• 142-61-0 Hexanoyl chloride 
• 1340546-31-7 diisopropyl 1-(4-bromobenzoyl)hydrazine-1,2-dicarboxylate 
• 19920-80-0 1-(4-bromophenyl)cyclohexan-1-ol 

Downstream Products

• 91800-85-0 α-<4-Brom-phenyl>-hexylamin 
• 431041-28-0 (-)-(S)-1-p-bromophenyl-1-hexanol 
• 431041-21-3 (-)-[(S)-1-(4-bromophenyl)hexyloxy]tert-butyldimethylsilane 
• 431041-23-5 (+)-(3'aS,4'S,5'R,6'aR)-[4'-[4-((S)-1''-(tert-butyldimethylsilanyloxy)hexyl)phenyl]-1',6'a,6',3'a-tetrahydro-5,5-dimethylspiro[1,3-dioxane-2,2']]pentalen-5'-ol 
• 431041-25-7 (-)-(3aS,4S,5R,6aR)-5-hydroxy-4-{4-[(S)-1'-(tert-butyldimethylsilanyloxy)hexyl]phenyl}-5-[tert-butyldimethylsilanyloxy]hexahydropentalen-2-one 
• 1006603-37-7 C₁₇H₂₅BrO₂ 
• 23703-22-2 1-bromo-4-n-hexylbenzene 
• 1123795-07-2 C₄₂H₄₂O₂ 
• 1116113-69-9 C₂₀H₃₃BrO 
• 1005164-68-0 C₂₄H₃₀ClNO₄S 
• 1065644-37-2 2,6-bis[2-(4-hexylphenyl)ethynyl]anthracene 
• 79887-11-9 4-hexylphenylacetylene 
• 259139-06-5 1-n-hexyl-4-(trimethylsilylethynyl)benzene 
• 38237-76-2 1-(4-aminophenyl)-hexan-1-one 

Relevant articles and documents

Preparation method of aryl ketone compound

The invention provides a preparation method of an aryl ketone compound, and belongs to the technical field of compound synthesis. The method comprises the following steps: under the action of a silver catalyst and water, carrying out reaction on aryl alkyne with a structure as shown in a formula 1 in a solvent at 60-120 DEG C for 12-48 hours, and separating and purifying a product after the reaction is finished, so as to obtain the single aryl ketone compound with a structure as shown in a formula I, the raw materials are easy to obtain, the experimental operation is simple, the yield of the prepared single aryl ketone compound is good, and gram-scale experiments can be carried out.

Chiral Dibenzopentalene-Based Conjugated Nanohoops through Stereoselective Synthesis

Conjugated nanohoops allow to investigate the effect of radial conjugation and bending on the involved π-systems. They can possess unexpected optoelectronic properties and their radially oriented π-system makes them attractive for host–guest chemistry. Be

Application of diphenylamino biphenyl carbonyl compounds to photocuring formula system

The invention relates to the technical field of novel material organic chemicals, in particular to a diphenylamino biphenyl carbonyl compound shown as a formula (I), a purpose of the compound as a radiation curing photoinitiator, and application purposes