71021-06-2 Usage
Uses
Used in Pharmaceutical Industry:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-S-phenyl-4-thiois used as a potential building block for the development of new pharmaceutical compounds due to its unique structure and the presence of phenyl and thio groups. These groups can be exploited for the synthesis of bioactive molecules with potential therapeutic applications.
Used in Organic Chemistry Research:
In the field of organic chemistry, .beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-S-phenyl-4-thiois used as a subject of interest for studying the properties and reactivity of hexose derivatives. Its unique structure allows researchers to explore new synthetic pathways and develop novel methodologies for the preparation of complex organic molecules.
Used in Biochemistry and Carbohydrate Chemistry:
.beta.-D-erythro-Hexopyranos-2-ulose, 1,6-anhydro-3-deoxy-4-S-phenyl-4-thiois also used in biochemistry and carbohydrate chemistry for understanding the role of hexose derivatives in biological systems. The presence of the phenyl and thio groups may provide insights into the interactions of these molecules with proteins and other biomolecules, potentially leading to the discovery of new biological activities and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 71021-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,2 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71021-06:
(7*7)+(6*1)+(5*0)+(4*2)+(3*1)+(2*0)+(1*6)=72
72 % 10 = 2
So 71021-06-2 is a valid CAS Registry Number.
71021-06-2Relevant academic research and scientific papers
Giri, Germán F.,Danielli, Mauro,Marinelli, Raúl A.,Spanevello, Rolando A.
, p. 3955 - 3957 (2016)
Levoglucosenone has been used as template for the synthesis of a wide variety of compounds with an impressive structural variability. However, scarce work has been done regarding the generation of new bioactive entities. Here we report the cytotoxic effec
