51673-83-7 Usage
Uses
Used in Pharmaceutical Research:
TETRAHYDROPYRAN-2-CARBOXYLIC ACID is used as a chiral building block for the synthesis of pharmaceuticals and other biologically active compounds, contributing to the development of new drugs with improved efficacy and selectivity.
Used in Drug Synthesis:
TETRAHYDROPYRAN-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals, enabling the creation of enantiomerically pure compounds with specific biological activities.
Used in Drug Delivery Systems:
TETRAHYDROPYRAN-2-CARBOXYLIC ACID is used in the development of novel drug delivery systems to improve the bioavailability, targeting, and therapeutic outcomes of pharmaceuticals.
Used in Organic Synthesis:
TETRAHYDROPYRAN-2-CARBOXYLIC ACID is used as a versatile intermediate in organic synthesis, facilitating the construction of complex molecular structures and controlling stereochemistry in various organic reactions.
Used in Therapeutic Applications:
TETRAHYDROPYRAN-2-CARBOXYLIC ACID has demonstrated potential therapeutic applications in the treatment of various diseases, offering new avenues for drug discovery and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 51673-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51673-83:
(7*5)+(6*1)+(5*6)+(4*7)+(3*3)+(2*8)+(1*3)=127
127 % 10 = 7
So 51673-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3/c7-6(8)5-3-1-2-4-9-5/h5H,1-4H2,(H,7,8)
51673-83-7Relevant academic research and scientific papers
Oxidation of partially protected carbohydrates at the nickel hydroxide electrode
Schaefer, Hans J.,Schneider, Roy
, p. 715 - 724 (2007/10/02)
Primary hydroxy groups in pyranoses are oxidized in excellent yields to the corresponding carboxylic acids. In furanose 3 the yield of acid is only moderate. Secondary hydroxy groups are inert, aside from lactols. The different reactivity of secondary and primary hydroxy groups allows the chemoselective oxidation of 8 and 10.
