334-29-2 Usage
Uses
Used in Pharmaceutical Industry:
Acetic acid 5-fluoropentyl ester is used as a solvent for the synthesis of various pharmaceutical compounds. Its properties as a clear, colorless liquid with a fruity odor make it suitable for dissolving a range of substances, facilitating the manufacturing process of different medications.
Used in Organic Compounds Production:
In the realm of organic chemistry, Acetic acid 5-fluoropentyl ester is utilized as a solvent in the production of a variety of organic compounds. Its ability to dissolve multiple substances aids in the synthesis and processing of these compounds, contributing to the advancement of organic chemistry.
Used in Synthetic Cannabinoids Production:
Although its use in this context is controversial and potentially hazardous, Acetic acid 5-fluoropentyl ester is sometimes used in the production of synthetic cannabinoids. These are psychoactive substances that mimic the effects of natural cannabinoids found in marijuana, and their synthesis may involve this ester as a component.
Check Digit Verification of cas no
The CAS Registry Mumber 334-29-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 334-29:
(5*3)+(4*3)+(3*4)+(2*2)+(1*9)=52
52 % 10 = 2
So 334-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H13FO2/c1-7(9)10-6-4-2-3-5-8/h2-6H2,1H3
334-29-2Relevant academic research and scientific papers
Investigating the Influence of (Deoxy)fluorination on the Lipophilicity of Non-UV-Active Fluorinated Alkanols and Carbohydrates by a New log P Determination Method
Linclau, Bruno,Wang, Zhong,Compain, Guillaume,Paumelle, Vincent,Fontenelle, Clement Q.,Wells, Neil,Weymouth-Wilson, Alex
supporting information, p. 674 - 678 (2016/02/23)
Property tuning by fluorination is very effective for a number of purposes, and currently increasingly investigated for aliphatic compounds. An important application is lipophilicity (log P) modulation. However, the determination of log P is cumbersome fo
Efficient SN2 fluorination of primary and secondary alkyl bromides by copper(I) fluoride complexes
Liu, Yanpin,Chen, Chaohuang,Li, Huaifeng,Huang, Kuo-Wei,Tan, Jianwei,Weng, Zhiqiang
, p. 6587 - 6592 (2013/12/04)
Copper(I) fluoride complexes ligated by phenanthroline derivatives have been synthesized and structurally characterized by X-ray crystallography. These complexes adopt as either ionic or neutral forms in the solid state, depending on the steric bulkiness of the substituent groups on the phenanthroline ligands. These complexes react with primary and secondary alkyl bromides to produce the corresponding alkyl fluorides in modest to good yields. This new method is compatible with a variety of important functional groups such as ether, thioether, amide, nitrile, methoxyl, hydroxyl, ketone, ester, and heterocycle moieties.
