50606-95-6

Basic information

• Product Name: 4-N-HEXYLBENZOYL CHLORIDE
• Synonyms: 4-hexyl-benzoylchlorid;4-HEXYLBENZOYL CHLORIDE;4-HEXYLBENZENE-1-CARBONYL CHLORIDE;4-N-HEXYLBENZOYL CHLORIDE;P-HEXYLBENZOYL CHLORIDE;4-n-Hexylbenzoylchloride,99%;4-Hexylbenzoic acid chloride;4-Hexylbenzoyl chloride,99%
• CAS NO: 50606-95-6
• Molecular Formula: C₁₃H₁₇ClO
• Molecular Weight: 224.73
• EINECS: 256-647-6
• Product Categories: Aromatic Halides (substituted);Acid Halides;Carbonyl Compounds;Organic Building Blocks
• Mol File: 50606-95-6.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 176-177°C 22mm
• Flash Point: >230 °F
• Appearance: clear yellow to light brown liquid
• Density: 1.029 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000835mmHg at 25°C
• Refractive Index: n20/D 1.5256(lit.)
• Sensitive: Moisture Sensitive
• BRN: 2208938
• CAS DataBase Reference: 4-N-HEXYLBENZOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-N-HEXYLBENZOYL CHLORIDE(50606-95-6)
• EPA Substance Registry System: 4-N-HEXYLBENZOYL CHLORIDE(50606-95-6)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 3265 8/PG 2
• WGK Germany: 3
• TSCA: Yes
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 50606-95-6(Hazardous Substances Data)

Usage

Description

4-N-HEXYLBENZOYL CHLORIDE is a clear yellow to light brown liquid that serves as an essential chemical intermediate in the synthesis of various organic compounds. It is characterized by its unique chemical structure, which allows it to participate in a range of chemical reactions and form different products.

Uses

Used in Chemical Synthesis:
4-N-HEXYLBENZOYL CHLORIDE is used as a chemical intermediate for the synthesis of various organic compounds. Its application is primarily due to its reactivity and ability to form new bonds with other molecules, leading to the creation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-N-HEXYLBENZOYL CHLORIDE is used as a key component in the synthesis of certain drugs. Its role is to provide the necessary chemical structure that can be further modified or combined with other molecules to create effective pharmaceutical agents.
Used in Material Science:
4-N-HEXYLBENZOYL CHLORIDE is also utilized in the field of material science, where it is employed in the development of new materials with specific properties. Its chemical structure allows it to be incorporated into polymers, coatings, and other materials, enhancing their performance and functionality.
Used in Research and Development:
4-N-HEXYLBENZOYL CHLORIDE is an important compound in research and development, where it is used to explore new chemical reactions and develop innovative applications. Its versatility and reactivity make it a valuable tool for scientists and researchers working on various projects.

InChI:InChI=1/C13H17ClO/c1-2-3-4-5-6-11-7-9-12(10-8-11)13(14)15/h7-10H,2-6H2,1H3

Upstream product

• 942-92-7 caprophenone 
• 142-61-0 Hexanoyl chloride 
• 71-43-2 benzene 
• 21643-38-9 4-hexylbenzoic acid 
• 79-37-8 oxalyl dichloride 
• 1077-16-3 hexylbenzene 

Downstream Products

• 64408-94-2 4-Hexyl-thiobenzoic acid S-(4-hexyl-phenyl) ester 
• 49763-69-1 4-hexylbenzaldehyde 
• 87741-45-5 4-Hexyl-benzoesaeure-<6-(4-methoxy-phenyl)-pyridazin-3-yl-ester> 
• 139674-83-2 N-(4-hexylbenzoyl)glycine 
• 118578-88-4 4-hexylphenylmethyl alcohol 
• 58999-67-0 1-chloromethyl-4-hexylbenzene 
• 60982-73-2 4-hexylphenylacetonitrile 
• 62808-19-9 4-hexylbenzoyloxy-4'-benzaldehyde 
• 77719-29-0 4-Hexyl-benzoic acid 4-(4-bromo-phenylethynyl)-phenyl ester 
• 74800-83-2 4-Hexyl-benzoic acid 4-(5-heptyl-[1,3]dioxan-2-yl)-phenyl ester 
• 93959-41-2 4-Hexyl-benzoic acid 4-[3-butyl-4-oxo-2-thioxo-thiazolidin-(5Z)-ylidenemethyl]-phenyl ester 
• 113423-32-8 2-(4-Hexyl-cyclohexyl)-5-(4-hexyl-phenyl)-[1,3,4]thiadiazole 
• 113423-31-7 2-(4-Hexyl-phenyl)-5-(4-pentyl-cyclohexyl)-[1,3,4]thiadiazole 
• 113423-30-6 2-(4-Butyl-cyclohexyl)-5-(4-hexyl-phenyl)-[1,3,4]thiadiazole 

Relevant articles and documents

Spiropyrane derivative with color, fluorescence and liquid crystal property triple switching effects as well as preparation method and application thereof

The invention discloses a spiropyrane derivative with color, fluorescence and liquid crystal property triple switching effects as well as a preparation method and application of the spiropyrane derivative. The spiropyrane derivative is prepared by esterification reaction of 1',3',3'-trimethyl-6-nitrospiro[benzopyran-2,2'-dihydroindole]-5', 8-diol and alkyl / alkoxy substituted benzoic acid with alkyl / alkoxy group at para-position or acrylate / methacrylate group at the chain end. The spiropyran derivative is used as a molecular switch in a smart material. The spiropyran derivative has responsiveness to light, heat, pH value and force, has triple switchable effects of color, fluorescence and liquid crystal property, has significant difference in response behaviors in different chemical environments, and is suitable for being used as a molecular switch in an intelligent material.

Benzyltin pyrimidine derivatives, their preparation and their use as medicaments

The invention relates to the field of pharmaceutical chemistry, specifically to benzyl pyrimidine derivatives (I), preparation methods thereof, medicinal compositions containing the derivatives and medical application of the derivatives, in particular, application of the derivatives as an immunosuppressant in autoimmune diseases and organ transplantation.

Preparation of new substituted bis(benzoyl) peroxides under aqueous conditions in the presence of stearyltrimethylammonium chloride

A series of new substituted bis(benzoyl) peroxides has been synthesised from their corresponding acid chlorides in high yield. The reactions were carried out in aqueous sodium peroxide solution and butanone in the presence of 0.5% stearyltrimethylammonium chloride (STAC) at a temperature below 15°C. STAC improved the purity, and the fast addition improved the yield of the peroxides. Mass spectral analysis of substituted bis(benzoyl) peroxides using EI has been carried out for accurate mass determinations. Springer-Verlag 2003.