16208-89-2 Usage
Uses
Used in Chemical Research:
2''-NITROPHENYL 2,2',3,3',4'-PENTA-O-ACETYL-B-D-XYLOBIOSIDE is used as a reagent for the study of carbohydrate chemistry due to its unique structure and properties that facilitate the analysis of complex carbohydrate structures.
Used in Carbohydrate Structure Analysis:
In the field of Carbohydrate Chemistry, 2''-NITROPHENYL 2,2',3,3',4'-PENTA-O-ACETYL-B-D-XYLOBIOSIDE is used as an analytical tool for understanding the structure and function of carbohydrates, which is crucial for advancing knowledge in glycobiology and related fields.
Used in Organic Synthesis:
2''-NITROPHENYL 2,2',3,3',4'-PENTA-O-ACETYL-B-D-XYLOBIOSIDE is utilized as a building block in organic synthesis, where its specific functional groups can be manipulated to create a variety of complex organic molecules for different applications.
Used in Pharmaceutical Development:
In the Pharmaceutical Industry, 2''-NITROPHENYL 2,2',3,3',4'-PENTA-O-ACETYL-B-D-XYLOBIOSIDE may be used as a precursor or intermediate in the synthesis of pharmaceutical compounds, particularly those targeting carbohydrate-based drug discovery.
Used in Biochemical Assays:
2''-NITROPHENYL 2,2',3,3',4'-PENTA-O-ACETYL-B-D-XYLOBIOSIDE is employed as a substrate or standard in biochemical assays to evaluate the activity of enzymes involved in carbohydrate metabolism or to study the interactions of carbohydrates with proteins and other biomolecules.
Check Digit Verification of cas no
The CAS Registry Mumber 16208-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,0 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16208-89:
(7*1)+(6*6)+(5*2)+(4*0)+(3*8)+(2*8)+(1*9)=102
102 % 10 = 2
So 16208-89-2 is a valid CAS Registry Number.
16208-89-2Relevant academic research and scientific papers
An efficient method for the synthesis of new derivatives of 2,4,6-triarylpyridines as cytotoxic agents
Baloutaki, Bahram Ahmadi,Sayahi, Mohammad Hosein,Nikpassand, Mohammad,Kefayati, Hassan
, p. 1153 - 1163 (2019/11/11)
New series of 2,4,6-triarylpyridines derivatives 5a–f and 6a–d were designed, synthesized and evaluated for their cytotoxic activity against breast cancer cell lines. Three-component reaction between acetophenones, ammonium acetate and 4-methyl or 2-methy
I2-Triggered N-O cleavage of ketoxime acetates for the synthesis of 3-(4-pyridyl)indoles
Gao, Qinghe,Wang, Yakun,Wang, Qianqian,Zhu, Yanping,Liu, Zhaomin,Zhang, Jixia
, p. 9030 - 9037 (2018/12/10)
A facile and complementary [3 + 2 + 1] annulation of aryl ketoxime acetates and 3-formylindoles to give pyridine derivatives is reported. The condensation reaction demonstrated that I2 was capable of triggering N-O bond cleavage of ketoxime ace
A porous metal-organic framework with helical chain building units exhibiting facile transition from micro- to meso-porosity
Park, Jinhee,Li, Jian-Rong,Carolina Sanudo,Yuan, Daqiang,Zhou, Hong-Cai
supporting information; experimental part, p. 883 - 885 (2012/02/01)
A metal-organic framework (MOF) with helical channels has been constructed by bridging helical chain secondary building units with 2,6-di-p-carboxyphenyl- 4,4′-bipyridine ligands. The activated MOF shows permanent porosity and gas adsorption selectivity. Remarkably, the MOF exhibits a facile transition from micro- to meso-porosity.
