15421-51-9 Usage
Description
[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid is a complex organic compound characterized by its unique stereochemistry and functional groups. It features a cyclohexyl ring with five hydroxyl groups and a phosphonic acid group attached to an oxygen atom. This structure endows the molecule with potential applications in various fields due to its ability to interact with other molecules through hydrogen bonding and electrostatic interactions.
Uses
Used in Pharmaceutical Applications:
[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid is used as a pharmaceutical agent for its potential therapeutic effects. The compound's hydroxyl and phosphonic acid groups allow it to interact with biological targets, such as enzymes and receptors, which may lead to the development of new drugs for various diseases.
Used in Agricultural Applications:
In the agricultural industry, [(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid is used as a component in the development of novel agrochemicals. Its ability to form complexes with metal ions and interact with biological molecules can be exploited to create compounds that target specific pests or enhance crop growth and yield.
Used in Chemical Synthesis:
[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid serves as a versatile building block in organic synthesis. Its unique stereochemistry and functional groups make it a valuable starting material for the synthesis of more complex molecules, such as natural products, pharmaceuticals, and advanced materials.
Used in Environmental Applications:
In the environmental sector, [(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid is used for its potential to sequester heavy metals and other pollutants. The compound's ability to form stable complexes with metal ions can be utilized in the development of new methods for environmental remediation and pollution control.
Used in Material Science:
[(2S,3R,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl]oxyphosphonic acid is used as a component in the development of new materials with unique properties. Its ability to form hydrogen bonds and interact with other molecules can be exploited to create materials with enhanced mechanical, thermal, or electrical properties for various applications, such as sensors, energy storage, and electronics.
Purification Methods
Crystallise the phosphate from water, and EtOH. Recrystallise 1g by dissolving it in 3mL of H2O and adding slowly 15mL of commercial EtOH, filter the crystals, wash with a little EtOH then Et2O and dry it in a vacuum. [McCormick & Carter Biochemical Preparations 2 65 1952.]
Check Digit Verification of cas no
The CAS Registry Mumber 15421-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,2 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15421-51:
(7*1)+(6*5)+(5*4)+(4*2)+(3*1)+(2*5)+(1*1)=79
79 % 10 = 9
So 15421-51-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H13O9P/c7-1-2(8)4(10)6(5(11)3(1)9)15-16(12,13)14/h1-11H,(H2,12,13,14)/t1-,2-,3-,4+,5-,6-/m1/s1
15421-51-9Relevant articles and documents
Divergent synthesis of all possible optically active regioisomers of myo-inositol mono- and bisphosphates
Seo, Kyung-Chang,Yu, Seok-Ho,Chung, Sung-Kee
, p. 305 - 327 (2008/02/12)
All possible optically active regioisomers of myo-inositol mono- and bisphosphates were synthesized using inositol derivatives suitably protected with various protecting groups (IRns) as key intermediates. A series of procedures including Novozym 435 cata
Kinetic resolution of d,l-myo-inositol derivatives catalyzed by chiral Cu(II) complex
Matsumura, Yoshihiro,Maki, Toshihide,Tsurumaki, Kazuya,Onomura, Osamu
, p. 9131 - 9134 (2007/10/03)
Kinetic resolution of d,l-myo-inositol derivatives having a 1,2-diol functionality by monobenzoylation was achieved using (R,R)-Ph-BOX-Cu(II) as a catalyst. The monobenzoylation preferentially took place at the 1,2-diol functionality via a highly enantiod
