109371-33-7 Usage
Uses
Used in Pharmaceutical Industry:
(S)-(-)-1-Benzyloxy-2-benzyloxy-3-tosyloxypropane is used as a chiral building block for the development of various pharmaceuticals. Its ability to impart asymmetry to target molecules makes it a valuable component in the synthesis of complex drug compounds, potentially leading to improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-(-)-1-Benzyloxy-2-benzyloxy-3-tosyloxypropane is utilized as a reagent in the synthesis of chiral agrochemicals. Its incorporation into these compounds can enhance their performance, targeting specific pests while minimizing harm to non-target organisms and the environment.
Used in Fine Chemicals Production:
(S)-(-)-1-Benzyloxy-2-benzyloxy-3-tosyloxypropane is also employed in the production of fine chemicals, such as flavors, fragrances, and dyes. Its unique structure and reactivity contribute to the creation of novel and diverse chemical compounds with specific properties, catering to various industrial needs.
Overall, (S)-(-)-1-Benzyloxy-2-benzyloxy-3-tosyloxypropane is a versatile and valuable compound in the fields of pharmaceuticals, agrochemicals, and fine chemicals production, thanks to its unique structure, reactivity, and ability to impart chirality to target molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 109371-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 109371-33:
(8*1)+(7*0)+(6*9)+(5*3)+(4*7)+(3*1)+(2*3)+(1*3)=117
117 % 10 = 7
So 109371-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H24O6S/c1-19-12-14-23(15-13-19)31(26,27)30-18-22(28-16-20-8-4-2-5-9-20)17-29-24(25)21-10-6-3-7-11-21/h2-15,22H,16-18H2,1H3/t22-/m0/s1
109371-33-7Relevant academic research and scientific papers
ENANTIOMERENREINE GLYCERIN-DERIVATE DURCH ENZYMATISCHE HYDROLYSE PROCHIRALER ESTER
Kerschner, V.,Kreiser, W.
, p. 531 - 534 (2007/10/02)
A practical method for large scale preparation of optical active glycerols protected in a versatile manner is described herein.Among these the crystalline pure enantiomers V deserve highest attention, since they offer three different functionalities for s
