1186623-24-4 Usage
Description
(R)-3-(4-bromophenoxy)propane-1,2-diol, with the molecular formula C9H11BrO3, is a chiral chemical compound that possesses a non-superimposable mirror image. This unique structure makes it a valuable compound in various fields, including organic synthesis and pharmaceutical development.
Uses
Used in Organic Synthesis:
(R)-3-(4-bromophenoxy)propane-1,2-diol is used as a reagent in organic synthesis for its ability to facilitate the formation of new chemical bonds and create a variety of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (R)-3-(4-bromophenoxy)propane-1,2-diol is used as a building block for the synthesis of new drugs and medications, thanks to its unique chiral structure and potential for chemical modification.
Used in Polymer Production:
(R)-3-(4-bromophenoxy)propane-1,2-diol has been studied for its potential use in the production of polymers and other materials, where its unique structure could contribute to the development of novel materials with specific properties.
Used in Chemical Research:
(R)-3-(4-bromophenoxy)propane-1,2-diol is of interest to researchers in the fields of chemistry and chemical engineering due to its unique structure, which offers opportunities for exploring new reactions and applications in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1186623-24-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,6,6,2 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1186623-24:
(9*1)+(8*1)+(7*8)+(6*6)+(5*6)+(4*2)+(3*3)+(2*2)+(1*4)=164
164 % 10 = 4
So 1186623-24-4 is a valid CAS Registry Number.
1186623-24-4Relevant articles and documents
Bacillus alcalophilus MTCC10234 catalyzed enantioselective kinetic resolution of aryl glycidyl ethers
Bala, Neeraj,Chimni, Swapandeep Singh,Saini, Harvinder Singh,Chadha, Bhupinder Singh
experimental part, p. 128 - 134 (2010/10/04)
The phenyl glycidyl ether derivatives have been kinetically resolved with the growing cells of Bacillus alcalophilus MTCC10234 yielding (S)-epoxides with up to >99% ee and (R)-diols with up to 89% ee. The enantiomeric ratio (E) of up to 67 has been obtained for biohydrolysis process. The effect of different substituents of phenyl glycidyl ether on the biocatalytic efficiency of B. alcalophilus MTCC10234 showed preference for methyl- and chloro-substituted aryl glycidyl ether derivatives whereas nitro-derivatives were transformed at a slower rate. 2,6-Dimethylphenyl glycidyl ether which contains a bulky aryl group having methyl group on both the ortho positions was resolved with an E=39.
