210358-01-3 Usage
Uses
Used in Pharmaceutical Industry:
BENZYL 2,3,4,6-TETRA-O-BENZYL-1-THIO-BETA-D-GALACTOPYRANOSIDE is used as a key intermediate in the synthesis of various complex carbohydrates and trisaccharides for pharmaceutical applications. Its unique structure allows for the development of novel drug candidates with potential therapeutic properties.
Used in Chemical Research:
In the field of chemical research, BENZYL 2,3,4,6-TETRA-O-BENZYL-1-THIO-BETA-D-GALACTOPYRANOSIDE serves as a valuable compound for studying the chemical properties and reactivity of saccharides. Its synthesis and modification can provide insights into the development of new synthetic methods and strategies for carbohydrate chemistry.
Used in Carbohydrate Synthesis:
BENZYL 2,3,4,6-TETRA-O-BENZYL-1-THIO-BETA-D-GALACTOPYRANOSIDE is used as a building block in the synthesis of more complex carbohydrate structures, such as oligosaccharides and polysaccharides. Its presence in these structures can influence their biological activity, making it an important compound for the development of new bioactive molecules.
Used in Material Science:
In material science, BENZYL 2,3,4,6-TETRA-O-BENZYL-1-THIO-BETA-D-GALACTOPYRANOSIDE can be utilized in the development of novel materials with unique properties. Its incorporation into polymers or other materials can lead to the creation of new materials with enhanced properties, such as improved biocompatibility or enhanced mechanical strength.
Check Digit Verification of cas no
The CAS Registry Mumber 210358-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,3,5 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 210358-01:
(8*2)+(7*1)+(6*0)+(5*3)+(4*5)+(3*8)+(2*0)+(1*1)=83
83 % 10 = 3
So 210358-01-3 is a valid CAS Registry Number.
210358-01-3Relevant academic research and scientific papers
Gold-catalysed glycosylation reaction using an easily accessible leaving group
Koppolu, Srinivasa Rao,Niddana, Ramana,Balamurugan, Rengarajan
, p. 5094 - 5097 (2015/05/13)
Gold(iii)-catalysed glycosylation reaction has been developed by employing a new and easily accessible leaving group synthesized from ethyl cyanoacetate. Several nucleophiles like alcohols, thiols, allyltrimethylsilane, trimethylsilyl azide and triethylsilane have been reacted to make the corresponding glycosides in good yields and with marginal to excellent α-selectivity. This journal is
1,2-trans-1-Dihydroxyboryl benzyl S-glycoside as glycosyl donor
Liu, Xiao,Zhang, Bingbing,Gu, Xiangying,Chen, Guohua,Chen, Lin,Wang, Xin,Xiong, Bing,You, Qi-Dong,Chen, Yue-Lei,Shen, Jingkang
, p. 45 - 49 (2015/01/30)
Activated by NBS, readily available 1,2-trans-1-dihydroxyboryl benzyl S-glycosides served as glycosyl donors and reacted with certain simple alcohol acceptors to produce pure 1,2-cis-O-glycosides in moderate yields. The boronic acid moiety was revealed es
A new route to exo-glycals using the Ramberg-Baecklund rearrangement
Griffin, Frank K.,Paterson, Duncan E.,Murphy, Paul V.,Taylor, Richard J. K.
, p. 1305 - 1322 (2007/10/03)
A new route to exo-glycals 4 is described in which glycosyl sulfones 3 are subjected to the Meyers variant of the Ramberg-Baecklund rearrangement. The conversion of sulfones derived from glucose, galactose, mannose, cellobiose, and ribose into di-, tri-, and tetra-substituted alkenes is reported. Preliminary mechanistic studies of this process are also described. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
