16844-08-9 Usage
Description
(S)-2-chlorooctane, with the molecular formula C8H17Cl, is a chiral compound that possesses a non-superimposable mirror image. Its stereochemistry is indicated by the (S) prefix in its name. This colorless liquid exhibits a strong, sweet odor and is recognized for its applications as a solvent, intermediate in chemical production, and reagent in organic synthesis.
Uses
Used in Chemical Synthesis:
(S)-2-chlorooctane is used as a solvent for facilitating various chemical reactions, particularly in the synthesis of other chemicals. Its properties as a solvent make it a valuable component in the chemical industry.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-2-chlorooctane is utilized as an intermediate. Its unique structure allows it to participate in a range of reactions, contributing to the creation of diverse chemical products.
Used in Laboratory Experiments:
(S)-2-chlorooctane also serves as a reagent in laboratory settings, where its specific chemical properties are harnessed for research and development purposes.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, due to its role in chemical synthesis and organic chemistry, (S)-2-chlorooctane could potentially be used in the pharmaceutical industry as a building block for the development of new drugs or drug candidates.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 16844-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,4 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16844-08:
(7*1)+(6*6)+(5*8)+(4*4)+(3*4)+(2*0)+(1*8)=119
119 % 10 = 9
So 16844-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H17Cl/c1-3-4-5-6-7-8(2)9/h8H,3-7H2,1-2H3/t8-/m0/s1
16844-08-9Relevant articles and documents
Iron(III)-catalyzed halogenations by substitution of sulfonate esters
Ortega, Nuria,Feher-Voelger, Andres,Brovetto, Margarita,Padron, Juan I.,Martin, Victor S.,Martin, Tomas
experimental part, p. 963 - 972 (2011/06/20)
A novel halogenation reaction from sulfonates catalyzed by iron(III) is described. The reaction can be performed as a stoichiometric or a catalytic version. This reaction provides a convenient strategy for the efficient access to structurally diverse secondary chlorides, bromides and iodides. The stereochemical course of the reaction is governed by the substrate and the experimental conditions. Secondary alcohols modified as quisylates or pysylates are substantially more reactive. Aliphatic quisylates proceed with overall inversion of configuration under catalytic conditions. Chemoselectivity in bismesylates was observed in favour of the secondary mesylate. Additionally, based on the experimental results, a possible catalytic cycle for the halogenation has been proposed.
