62414-75-9 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is used as a potential drug candidate for its anticancer properties. It has been the subject of research for its ability to target and inhibit the growth of cancer cells, making it a promising agent in the fight against various types of cancer.
Used in Antifungal Applications:
In the field of antifungal research, 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is utilized for its potential to combat fungal infections. Its antifungal properties are being studied to develop new treatments for various fungal diseases.
Used in Bioactive Compound Development:
2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is employed in the development of new bioactive compounds. Its unique structure and properties make it a valuable component in the creation of innovative pharmaceuticals and therapeutic agents.
Used in Research and Development:
In the scientific community, 2,3,4-TRI-O-ACETYL-ALPHA-D-ARABINOPYRANOSYL ISOTHIOCYANATE is used as a subject of research to explore its potential benefits and applications. Further studies are needed to understand its full potential and to unlock its capabilities in various fields of medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 62414-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62414-75:
(7*6)+(6*2)+(5*4)+(4*1)+(3*4)+(2*7)+(1*5)=109
109 % 10 = 9
So 62414-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO7S/c1-6(14)18-9-4-17-12(13-5-21)11(20-8(3)16)10(9)19-7(2)15/h9-12H,4H2,1-3H3/t9-,10-,11+,12+/m1/s1
62414-75-9Relevant academic research and scientific papers
A simple method for the preparation of glycosyl isothiocyanates
Kuehne, Marco,Gyoergydeak, Zoltan,Lindhorst, Thisbe K.
, p. 949 - 951 (2007/10/03)
Glycosyl isothiocyanates became accessible from the corresponding peracetylated sugars in one step, by application of trimethylsilyl isothiocyanate and a Lewis acid in dichloromethane at room temperature. Georg Thieme Verlag Stuttgart.
Solvent-free preparation of glycosyl isothiocyanates
Lindhorst,Kieburg
, p. 1228 - 1230 (2007/10/02)
By a novel solvent-free procedure, peracetylated glycosyl bromides are reacted with potassium thiocyanate in the melt to give the corresponding glycosyl isothiocyanates. The method is applicable to several glycosyl bromides tested, including classical hexoses and pentoses, deoxy sugars and even disaccharides. No glycosyl thiocyanates are obtained. In general, the glycosyl isothiocyanates are formed stereoselectively having 1,2-trans configuration in yields between 41-74%.
STUDIES ON NUCLEOSIDE ANALOGS. XXIV. MONO- AND DISACCHARIDE ISOTHIOCYANATES
Ogura, Haruo,Takahashi, Hiroshi
, p. 87 - 90 (2007/10/02)
The reaction of mono- and disaccharide bromide with Pb(SCN)2 or AgSCN in dry benzene or benzene-toluene gives the respective mono- and disaccharide isothiocyanates and the confirmation of their stereochemistry of mono- and disaccharide isothiocyanates is
