19200-24-9 Usage
Uses
Used in Organic Chemistry:
.beta.-D-Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(dimethylcarbamodithioate) is used as a reagent in organic chemistry for the synthesis of various complex organic molecules. Its unique structure allows for specific reactions and transformations, making it a valuable tool in the development of new compounds and materials.
Used in Biochemistry:
In biochemistry, .beta.-D-Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(dimethylcarbamodithioate) is used as a research tool to study the interactions and mechanisms of sugar-based molecules with biological systems. Its unique structure can help researchers understand the role of sugar molecules in biological processes and their potential as therapeutic agents.
Used in Pharmaceutical Research:
.beta.-D-Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(dimethylcarbamodithioate) is used as a starting material or intermediate in the development of new pharmaceutical compounds. Its unique structure and potential reactivity make it a promising candidate for the design and synthesis of novel drugs targeting various diseases and conditions.
Further study and analysis may be required to fully understand the properties and potential uses of .beta.-D-Glucopyranose, 1-thio-, 2,3,4,6-tetraacetate 1-(dimethylcarbamodithioate) in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19200-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,0 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19200-24:
(7*1)+(6*9)+(5*2)+(4*0)+(3*0)+(2*2)+(1*4)=79
79 % 10 = 9
So 19200-24-9 is a valid CAS Registry Number.
19200-24-9Relevant academic research and scientific papers
A protecting group-free approach for synthesizingC-glycosides through glycosyl dithiocarbamates
Li, Gefei,Noguchi, Masato,Arisaka, Genki,Tanaka, Yuuki,Shoda, Shin-Ichiro
supporting information, p. 3134 - 3138 (2021/04/21)
The first protection/deprotection-free process for radicalC-glycosylation has been achieved through one-step preparable glycosyl dithiocarbamates (GDTCs). The Giese-type reaction and radical allylation of unprotected GDTCs were successfully performed to obtain the corresponding α-C-glycosides stereoselectively under mild reaction conditions.
