470-14-4 Usage
Description
2-Pentanone, 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)is a colorless, highly reactive compound that contains a ketone group and four hydroxyl groups. It has a chemical formula of C5H12O5 and is soluble in water and other organic solvents. 2-Pentanone, 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)is known for its ability to act as a chelating agent, forming complexes with metal ions. Due to its unique chemical structure, it has a variety of potential applications in the fields of medicine, chemical engineering, and industry.
Uses
Used in Pharmaceutical Synthesis:
2-Pentanone, 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)is used as an intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs and medications.
Used in Chemical Engineering:
In the field of chemical engineering, 2-Pentanone, 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)is used as a chelating agent. Its ability to form complexes with metal ions makes it useful in various chemical processes, such as the removal of metal impurities or the stabilization of certain compounds.
Used in Industrial Applications:
2-Pentanone, 1,3,4,5-tetrahydroxy-4-(hydroxymethyl)also has potential applications in various industries. Its solubility in water and organic solvents, along with its reactivity, makes it a valuable component in the development of new materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 470-14-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 470-14:
(5*4)+(4*7)+(3*0)+(2*1)+(1*4)=54
54 % 10 = 4
So 470-14-4 is a valid CAS Registry Number.
470-14-4Relevant articles and documents
Aldol type reaction of unprotected sugars in methanol
Saimoto, Hiroyuki,Yatani, Setsuo,Sashiwa, Hitoshi,Shigemasa, Yoshihiro
, p. 937 - 938 (2007/10/02)
Although aldol condensation of 1,3-dihydroxyacetone with formaldehyde in methanol catalyzed by CaCl2/KOH gave glycero-tetrulose, the reaction catalyzed by Ca(OH)2 preferentially gave 1,3-dihydroxyacetone dimer. The result was explained by the formation of a chelated enolate. This sequence was successfully applied to the stereoselective synthesis of threo-3-pentulose.
Kinetics, Catalysis, and Mechanism of the Secondary Reaction in the Final Phase of the Formose Reaction
Harsch, Guenther,Bauer, Hermann,Voelter, Wolfgang
, p. 623 - 635 (2007/10/02)
In the final phase of the formose reaction sugars are formed by the reaction of glycolaldehyde, glyceraldehyde and dihydroxyacetone.The application of high-pressure liquid chromatography allows for the first time to investigate intermediate and final products quantitatively.The results of kinetical investigations allow to suggest a reaction mechanism for the secondary reaction in the final phase of the formose reaction.This mechanism is compared with that of the starting phase and other known mechanisms.From the results metal ion-catalyzed aldol reactions have to be assumed.
