151909-88-5 Usage
Description
2,3,4-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-L-fucopyranose, with the CAS number 151909-88-5, is an off-white solid compound that is primarily utilized in the field of organic synthesis. It is a derivative of L-fucopyranose, a monosaccharide, with three benzyl groups attached to the 2, 3, and 4 positions, and a 4-nitrobenzoyl group attached to the 1 position. This structural arrangement endows the compound with unique chemical properties that make it valuable for various applications in organic chemistry.
Uses
Used in Organic Synthesis:
2,3,4-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-L-fucopyranose is used as an intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for selective functionalization and modification, making it a versatile building block for the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3,4-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-L-fucopyranose is used as a key intermediate in the synthesis of novel drug candidates. Its structural diversity and the ability to undergo various chemical transformations make it an attractive starting material for the development of new therapeutic agents with potential applications in the treatment of various diseases and medical conditions.
Used in Research and Development:
2,3,4-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-L-fucopyranose is also used as a research tool in academic and industrial laboratories. Its unique chemical properties and reactivity make it an ideal compound for studying various organic reactions and exploring new synthetic methodologies. Additionally, it can be employed in the development of new analytical techniques and methods for the characterization of complex organic molecules.
Used in Material Science:
In the field of material science, 2,3,4-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-L-fucopyranose can be used as a building block for the development of novel materials with specific properties. Its unique structure and functional groups can be exploited to create materials with tailored characteristics, such as improved mechanical strength, thermal stability, or specific interactions with other molecules, which can find applications in various industries, including electronics, aerospace, and automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 151909-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,9,0 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151909-88:
(8*1)+(7*5)+(6*1)+(5*9)+(4*0)+(3*9)+(2*8)+(1*8)=145
145 % 10 = 5
So 151909-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C34H33NO8/c1-24-30(39-21-25-11-5-2-6-12-25)31(40-22-26-13-7-3-8-14-26)32(41-23-27-15-9-4-10-16-27)34(42-24)43-33(36)28-17-19-29(20-18-28)35(37)38/h2-20,24,30-32,34H,21-23H2,1H3/t24?,30-,31+,32+,34+/m1/s1
151909-88-5Relevant articles and documents
Preferred Conformation of C-glycosides. 10. Synthesis and Conformational Analysis of Carbon Trisaccharides
Haneda, Toru,Goekjian, Peter G.,Kim, Sung H.,Kishi, Yoshito
, p. 490 - 498 (2007/10/02)
A flexible and efficient synthesis of the carbon trisaccharide 2 related to the Type II (O)H blood group determinant has been developed.This route was applied to the synthesis of the trisaccharides 3, 4, and 5.The preferred solution conformations of compo
