170210-39-6 Usage
Description
(2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate is a chiral compound with a complex structure that features multiple functional groups, including bromomethyl, dichlorophenyl, dioxolan, and methyl benzoate. Its (2R,4R) configuration indicates the presence of two stereocenters, making it optically active. (2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate's reactivity, stemming from the bromomethyl group, positions it for use in organic synthesis and as a reagent in various chemical reactions. The diverse functional groups present in the molecule suggest a broad spectrum of potential applications, particularly in the pharmaceutical and chemical industries.
Uses
Used in Organic Synthesis:
(2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate is used as a reactive intermediate in organic synthesis for the creation of new compounds and materials. Its bromomethyl group facilitates various chemical reactions, making it a versatile building block for the development of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate is used as a key component in the synthesis of drug candidates. Its unique structure and functional groups can be leveraged to design molecules with specific biological activities, potentially leading to the discovery of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
(2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate is utilized in chemical research as a probe to study reaction mechanisms and to develop new synthetic methodologies. Its optical activity and complex structure make it an interesting subject for investigations into stereoselective synthesis and the exploration of novel reaction pathways.
Used in Agrochemical Development:
In agrochemical development, (2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate is employed as a starting material for the synthesis of new pesticides and other crop protection agents. Its structural features can be tailored to target specific pests or diseases, potentially offering more effective and environmentally friendly solutions for agriculture.
Used in Specialty Chemicals Production:
(2R,4R)-(+)-<2-(bromomethyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl>methyl benzoate is used in the production of specialty chemicals, such as fragrances, dyes, and coatings. Its unique properties can contribute to the creation of high-value products with specific performance characteristics, catering to niche market demands.
Check Digit Verification of cas no
The CAS Registry Mumber 170210-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,2,1 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 170210-39:
(8*1)+(7*7)+(6*0)+(5*2)+(4*1)+(3*0)+(2*3)+(1*9)=86
86 % 10 = 6
So 170210-39-6 is a valid CAS Registry Number.
170210-39-6Relevant articles and documents
Stereoselective Syntheses of Both Enantiomers of Ketoconazole from (R)- and (S)-Epichlorohydrin
Camps, Pelayo,Farres, Xavier,Garcia, Luisa,Ginesta, Joan,Pascual, Jaume,et al.
, p. 1283 - 1294 (2007/10/03)
Stereoselective syntheses of both enantiomers of ketoconazole (1) from commercially available (R)- or (S)-epichlorohydrin has been developed.The key-step of syntheses involves the selective substitution of the methylene chlorine atom by benzoate on a mixture of (2S,4R)-14a and (2R,4R)-15a or of their enentiomers, followed by crystalization of the corresponding cis-benzoates, (2R,4R)-18 or (2S,4S)-18, from which (+)- or (-)-1 were obtained as described for (+/-)-1.The ee's of (+)- and (-)-ketocanazole were determined by HPLC on the CSP Chiracel OD-H.
