10140-96-2 Usage
Description
Ethyl 6-chlorohexanoate is an organic compound that serves as an important intermediate in the synthesis of various pharmaceuticals and chemicals. It is characterized by its ability to introduce a hexanoic acid group or ester into other compounds, which is crucial for the development of specific chemical structures.
Uses
Used in Pharmaceutical Synthesis:
Ethyl 6-chlorohexanoate is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its ability to add a hexanoic acid group or ester allows for the creation of specific chemical structures that are essential in the development of drugs with targeted therapeutic effects.
Used in Chemical Synthesis:
In the chemical industry, ethyl 6-chlorohexanoate is utilized as a key component in the synthesis of a range of compounds, such as 4-Morpholinehexanoic acid Hydrochloride and Ethyl 2,3-Dihydro-4-methyl-2-oxo-5-thiazolehexanoate. These compounds find applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Overall, ethyl 6-chlorohexanoate plays a significant role in the synthesis of various compounds, particularly in the pharmaceutical and chemical industries, due to its unique ability to introduce a hexanoic acid group or ester into other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 10140-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10140-96:
(7*1)+(6*0)+(5*1)+(4*4)+(3*0)+(2*9)+(1*6)=52
52 % 10 = 2
So 10140-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H15ClO2/c1-2-11-8(10)6-4-3-5-7-9/h2-7H2,1H3
10140-96-2Relevant articles and documents
ROMPgel-Supported Triphenylphosphine with Potential Application in Parallel Synthesis
Arstad, Erik,Barrett, Anthony G. M.,Hopkins, Brian T.,Koebberling, Johannes
, p. 1975 - 1977 (2002)
(Equation Presented) ROMPgel-supported triphenylphosphine was synthesized in three steps (67%) from norbornadiene, 4-bromoiodobenzene, and chlorodiphenylphosphine. The supported reagent has a high loading (2.5 mmol/g) and favorable swelling properties in organic solvents. It has been utilized for the conversion of alcohols to halides, the reduction of ozonides, and the isomerization of α,β-acetylenic esters and in the Staudinger reaction. In general, filtration of the resin from the reaction mixtures and evaporation gave the corresponding products in high yield and purity.
A mild, phosphine-free method for the conversion of alcohols into halides (Cl, Br, I) via the corresponding O-alkyl isoureas
Li, Zhengning,Crosignani, Stefano,Linclau, Bruno
, p. 8143 - 8147 (2007/10/03)
A novel procedure for the conversion of primary and secondary alcohols into the corresponding alkyl chlorides, bromides and iodides is described. The transformation is high-yielding in the case of chlorides and bromides, tolerates a range of functional groups, and does not rely on the use of phosphines.
