102719-14-2 Usage
Uses
Used in Pharmaceutical Industry:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate is used as a starting material for the synthesis of various drug compounds, taking advantage of its unique structural properties to create novel pharmaceutical agents.
Used in Organic Chemistry Research:
In the field of organic chemistry, .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-, 2-acetate serves as a valuable compound for studying carbohydrate derivatives, contributing to the understanding of their chemical behavior and potential applications in drug development and chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 102719-14-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 102719-14:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*4)=92
92 % 10 = 2
So 102719-14-2 is a valid CAS Registry Number.
102719-14-2Relevant 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
