141607-35-4 Usage
Uses
Used in Organic Synthesis:
5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is used as a building block in organic synthesis for its stability and ease of manipulation, allowing for the creation of various complex organic molecules.
Used in Carbohydrate Chemistry:
In carbohydrate chemistry, 5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is used as a protected form of D-ribose, facilitating the synthesis of complex carbohydrate structures.
Used in Pharmaceutical Synthesis:
5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and bioactive molecules.
Used in the Synthesis of Bioactive Molecules:
5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is employed in the synthesis of bioactive molecules, playing a crucial role in the discovery and production of substances with potential therapeutic applications.
Used in the Synthesis of Natural Products:
5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is used as a key intermediate in the synthesis of natural products, aiding in the replication and modification of naturally occurring compounds for various applications.
Used in the Preparation of Nucleosides, Nucleotides, and Glycosides:
5-O-tert-Butyldiphenylsilyl-2,3-O-isopropylidene-D-ribofuranose is utilized as a building block in the preparation of nucleosides, nucleotides, and glycosides, which are essential components of biological systems and have significant roles in molecular biology and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 141607-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,0 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141607-35:
(8*1)+(7*4)+(6*1)+(5*6)+(4*0)+(3*7)+(2*3)+(1*5)=104
104 % 10 = 4
So 141607-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C25H34O4Si/c1-24(2,3)30(19-12-8-6-9-13-19,20-14-10-7-11-15-20)27-17-18-16-21(26)23-22(18)28-25(4,5)29-23/h6-15,18,21-23,26H,16-17H2,1-5H3/t18-,21u,22-,23?/m1/s1
141607-35-4Relevant academic research and scientific papers
First total synthesis and structure confirmation of diacetylenic polyol (+)-oploxyne B
Srihari,Sathish Reddy,Yadav,Yedlapudi,Kalivendi, Shasi V.
supporting information, p. 5616 - 5618 (2013/09/23)
The first total synthesis of the natural product (+)-oploxyne B is achieved. The synthesis has led to the confirmation of absolute stereochemistry of the natural product. The natural product displayed cytotoxic activity with IC50 values varying
