15397-16-7 Usage
Uses
Used in Pharmaceutical Industry:
D-Ribofuranose is used as a key component in the synthesis of nucleotides for its role in the production of RNA and DNA, which are essential for genetic information storage and expression.
Used in Biochemical Research:
D-Ribofuranose is used as a research tool for studying the structure and function of nucleotides, coenzymes, and other biomolecules that are vital for cellular processes.
Used in Nutritional Supplements:
D-Ribofuranose is used as a dietary supplement to support energy production and overall health, given its role in the synthesis of essential coenzymes and its presence in important biomolecules.
Used in Food and Beverage Industry:
D-Ribofuranose may be used in the formulation of food and beverages to enhance nutritional content, particularly as a source of riboflavin (vitamin B2), which is important for energy metabolism and maintaining healthy vision, skin, and mucous membranes.
Used in Cosmetics and Personal Care Products:
D-Ribofuranose could be incorporated into cosmetics and personal care products for its potential antioxidant properties, contributing to skin health and protection against oxidative stress.
Check Digit Verification of cas no
The CAS Registry Mumber 15397-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,9 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15397-16:
(7*1)+(6*5)+(5*3)+(4*9)+(3*7)+(2*1)+(1*6)=117
117 % 10 = 7
So 15397-16-7 is a valid CAS Registry Number.
InChI:InChI=1/C34H28O9/c1-34(43-32(38)26-20-12-5-13-21-26)28(41-30(36)24-16-8-3-9-17-24)27(22-39-29(35)23-14-6-2-7-15-23)40-33(34)42-31(37)25-18-10-4-11-19-25/h2-21,27-28,33H,22H2,1H3/t27-,28-,33-,34-/m1/s1
15397-16-7Relevant academic research and scientific papers
2′-C-alkylribonucleosides: Design, synthesis, and conformation
Harry-O'kuru, Rogers E.,Kryjak, Emily A.,Wolfe, Michael S.
, p. 1457 - 1460 (2007/10/03)
Certain 2′-C-alkylribonucleotides have been designed as potential mechanism-based inactivators of ribonucleotide reductases. A short, flexible route toward the corresponding nucleosides and NMR evidence concerning their preferred solution conformations are discussed. Copyright
A concise synthesis of 2'-C-methylribonucleosides
Wolfe,Harry-O'kuru
, p. 7611 - 7614 (2007/10/02)
2'-C-methylribonucleosides were synthesized in five steps from commercially available 1,3,5-tri-O-benzoyl-α-D-ribose with good overall yields.
