117470-90-3 Usage
Uses
Used in Pharmaceutical Industry:
DIMETHYL L-TARTRATE CYCLIC SULFATE is used as a chiral resolving agent for the separation of enantiomers, which is crucial in the development of single-enantiomer drugs. The ability to separate enantiomers ensures that pharmaceuticals can be more effectively and safely targeted to treat specific conditions.
Used in Food Industry:
In the food industry, DIMETHYL L-TARTRATE CYCLIC SULFATE is utilized for its properties that can enhance or alter the taste and texture of food products, contributing to the development of innovative food formulations.
Used in Organic Synthesis:
DIMETHYL L-TARTRATE CYCLIC SULFATE is used as a reagent in organic synthesis, facilitating the creation of new compounds and molecules that can be applied across various fields, including materials science and pharmaceuticals.
Used in Drug Development:
It is being explored for its potential applications in drug development, where its unique properties may contribute to the discovery of new therapeutic agents and improve the efficacy of existing medications.
Used as a Catalyst in Chemical Reactions:
Due to its reactivity, DIMETHYL L-TARTRATE CYCLIC SULFATE is also considered for use as a catalyst in various chemical reactions, potentially streamlining processes and enhancing yields in the synthesis of complex molecules.
DIMETHYL L-TARTRATE CYCLIC SULFATE's multifaceted applications underscore its importance in contributing to the advancement of pharmaceutical and chemical research and development, making it a compound of significant interest in the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 117470-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,4,7 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117470-90:
(8*1)+(7*1)+(6*7)+(5*4)+(4*7)+(3*0)+(2*9)+(1*0)=123
123 % 10 = 3
So 117470-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O8S/c1-11-5(7)3-4(6(8)12-2)14-15(9,10)13-3/h3-4H,1-2H3/t3-,4-/m1/s1
117470-90-3Relevant academic research and scientific papers
Shangguan, Ning,Joullié, Madeleine
, p. 6748 - 6750 (2009)
A one-step copper-carbodimide elimination was used to provide the (E)-dehydroisoleucine moiety in the phomopsin side chain stereoselectively. An efficient approach to the phomopsin tripeptide side chain was developed to be used in the total syntheses of p
