2323-81-1

Basic information

• Product Name: Pentanoic acid, 5-chloro-, ethyl ester
• CAS NO: 2323-81-1
• Molecular Formula: C7H13ClO2
• Molecular Weight: 164.632
• Mol File: 2323-81-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Pentanoic acid, 5-chloro-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Pentanoic acid, 5-chloro-, ethyl ester(2323-81-1)
• EPA Substance Registry System: Pentanoic acid, 5-chloro-, ethyl ester(2323-81-1)

Safety Data

• Hazardous Substances Data: 2323-81-1(Hazardous Substances Data)

Usage

General Description

Pentanoic acid, 5-chloro-, ethyl ester is a chemical compound that is used in various applications, including as a flavoring agent in food and beverage products. It is also used in the pharmaceutical industry as an intermediate for the production of active pharmaceutical ingredients. Pentanoic acid, 5-chloro-, ethyl ester is known for its fruity and sweet aroma, and it is often used in the production of perfumes and fragrances. Additionally, it is used as a solvent in some industrial processes. However, it is important to handle this compound with care, as it can be harmful if ingested, inhaled, or comes into contact with the skin.

Upstream product

• 64-17-5 ethanol 
• 6280-87-1 δ-chlorovaleronitrile 
• 1119-46-6 5-chloro-valeric acid 
• 542-28-9 3,4,5,6-tetrahydro-2H-pyran-2-one 
• 623-73-4 diazoacetic acid ethyl ester 
• 121481-63-8 5-ethoxy-valeryl chloride 

Downstream Products

• 53007-36-6 1,1,5-pentanetricarboxylic acid triethyl ester 
• 5259-98-3 5-chloropentan-1-ol 
• 2323-74-2 <δ-Aethoxycarbonyl-butyl>-phosphonsaeure-diaethylester 
• 7035-28-1 5-Chlor-1,1-bis-(4-fluorphenyl) pentanol 
• 2050-20-6 diethyl pimelate 
• 7035-13-4 (5-chloropent-1-ene-1,1-diyl)dibenzene 
• 7035-14-5 (5-chloropentane-1,1-diyl)dibenzene 
• 7035-29-2 5-Chlor-1,1-bis(4-fluorphenyl)-1-penten 
• 98977-38-9 ethyl (+/-)-1-(tert-butyloxycarbonyl)-3-oxoperhydroazepine-4-carboxylate 
• 124932-43-0 (R)-(+)-3-Amino-hexahydro-1H-azepin 
• 643045-39-0 C₈H₁₆N₂O 
• 146407-32-1 1-benzylazepan-3-one 
• 870842-23-2 3-oxoazepane-1-carboxylic acid tert-butyl ester 
• 171257-01-5 ε-caprolactam 

Relevant articles and documents

Copper-catalyzed radical ring-opening halogenation with HX

An efficient copper-catalyzed radical ring-opening halogenation with HX (aq) is described. This protocol features redox-neutral conditions, green halogen sources, and a broad substrate scope, providing practical access to distally chlorinated, brominated and iodinated alkyl ketones and alkyl nitriles with moderate to good yields. This journal is

Reactions of CF3-substituted boranes with α-diazocarbonyl compounds

Boranes substituted with a CF3-group can be generated from methyl boronic esters RB(OMe)2 and Me3SiCF3/KF followed by treatment with Me3SiCl. These boranes are stable only in coordinating solvents, and due to the increased Lewis acidity of boron, react rapidly with α-diazocarbonyl compounds to give the products of transfer of the organic group from boron. Alkyl, aryl, vinyl, and alkynyl boronic esters can be used in this reaction.