102719-15-3 Usage
Uses
Used in Pharmaceutical Industry:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate is used as a building block for the production of various pharmaceuticals. Its unique structure and properties make it a valuable component in the synthesis of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate is used as a building block for the production of various agrochemicals. Its versatility and stability contribute to the development of effective and sustainable products for agricultural applications.
Used in Material Science:
.beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate has potential applications in the development of new materials. Its unique properties and structure can be utilized to create innovative materials with specific characteristics for various industries.
Used in Biochemical Research:
As a reagent in biochemical research, .beta.-D-ribo-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate can be used to study various biological processes and interactions. Its potential biological activities make it an interesting candidate for further research in the field of medicine and biology.
Check Digit Verification of cas no
The CAS Registry Mumber 102719-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,1 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102719-15:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*5)=93
93 % 10 = 3
So 102719-15-3 is a valid CAS Registry Number.
102719-15-3Relevant academic research and scientific papers
Manipulating the enone moiety of levoglucosenone: 1,3-Transposition reactions including ones leading to isolevoglucosenone
Ma, Xinghua,Liu, Xin,Yates, Patrick,Raverty, Warwick,Banwell, Martin G.,Ma, Chenxi,Willis, Anthony C.,Carr, Paul D.
, p. 5000 - 5011 (2018/06/20)
The manipulation of the enone moiety associated with the biomass-derived, homochiral and now abundant compound levoglucosenone (1) is described. While the trichloroacetimidates derived from the allylic alcohols 3 and 4 failed to engage in Overman-type rea
SYNTHESIS AND THERMAL CHEMISTRY OF ISOLEVOGLUCOSENONE
Furneaux, Richard H.,Gainsford, Graeme J.,Shafizadeh, Fred,Stevenson, Thomas T.
, p. 113 - 128 (2007/10/02)
Isolevoglucosenone (1,6-anhydro-2,3-dideoxy-β-D-glycero-hex-2-enopyranos-4-ulose, 3) has been synthesized from levoglucosenone (2) in six steps.Thus, 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose, obtained by Michael addition of benzyl al
