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D-ribonic acid 5-phosphate, also known as D-ribulose 5-phosphate, is an important organic compound that plays a crucial role in various metabolic pathways within living organisms. It is a key intermediate in the pentose phosphate pathway, which is essential for the generation of NADPH, a vital coenzyme involved in reductive biosynthesis and antioxidant defense. D-ribonic acid 5-phosphate is formed through the isomerization of D-ribulose 5-phosphate by the enzyme ribulose-phosphate 3-epimerase. D-ribonic acid 5-phosphate is also involved in the Calvin cycle, a series of biochemical reactions that occur in the chloroplasts of plants, algae, and some bacteria, facilitating the fixation of carbon dioxide into organic molecules. The significance of D-ribonic acid 5-phosphate lies in its ability to participate in these critical metabolic processes, contributing to energy production and the synthesis of essential biomolecules.

7424-07-9

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7424-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7424-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7424-07:
(6*7)+(5*4)+(4*2)+(3*4)+(2*0)+(1*7)=89
89 % 10 = 9
So 7424-07-9 is a valid CAS Registry Number.

7424-07-9Downstream Products

7424-07-9Relevant academic research and scientific papers

KINETICS AND MECHANISM OF OXIDATION OF D-GLUCOPYRANOSE 6-PHOSPHATE AND D-RIBOFURANOSE 5-PHOSPHATE BY VANADIUM(V) IN PERCHLORIC ACID MEDIA

Gupta, Kalyan Kali Sen,Gupta, Shipra Sen,Mandal, Subrata Kumar,Basu, Samarendra Nath

, p. 193 - 200 (1986)

The second-order rate constants for the oxidations of D-glucopyranose 6-phosphate and D-ribofuranose 5-phosphate by vanadium(V) in perchloric acid media have been measured spectrophotometrically in the visible region.The order with respect to +> is less than unity for each reaction.The enthalpy and entropy of activations of the reactions are higher than those for the corresponding two-electron oxidations by chromium(VI).The oxidations involve free-radical intermediates.

Reactivity of some sugars and sugar phosphates towards gold(III) in sodium acetate-acetic acid buffer medium

Sen Gupta, Kalyan Kali,Pal, Biswajit,Begum, Bilkis Ara

, p. 115 - 123 (2007/10/03)

The kinetics of the oxidation of some aldoses and aldose phosphates have been studied spectrophotometrically in sodium acetate-acetic acid buffer medium at different temperatures. The reactions are first order with respect to [Au(III)] and [substrate]. Both H+ and Cl- ions retard the reaction. The reactions appear to involve different gold(III) species, viz. AuCl4/-, AuCl3(OH2) and AuCl3(OH)-. The results are interpreted in terms of the probable intermediate formation of free radicals and Au(II). Aldoses react with gold(III) in the order: triose > tetrose > pentose > hexose. The sugar phosphates react with gold(III) at a faster rate than the parent sugars except glucose-1-phosphate, which reacts at slower rates than glucose. A tentative reaction mechanism leading to the formation of products has been suggested.

Reactivities of some sugar phosphates towards permanganate in perchloric acid medium and mechanism of the oxidation processes

Sen Gupta, Kalyan Kali,Tribedi, Partha Sarathi,Sen Gupta, Shipra

, p. 427 - 430 (2007/10/03)

The reactivities of some sugar phosphates towards permanganate have been examined in perchloric acid medium. The reactions are first order in [sugar phosphate] and [MnO4-]. The rate increases with increase in [H+]. The reactivities follow the order: erythrose 4-phosphate> ribose 5-phosphate> fructose 1,6-diphosphate> glucose 6-phosphate> glucose 1-phosphate. The mechanism of the reactions is discussed.

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