102719-11-9 Usage
Uses
Used in Pharmaceutical Industry:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)is used as a building block for the synthesis of complex molecules and pharmaceutical compounds due to its unique structure and chemical properties. Its potential applications in drug synthesis can contribute to the development of new medications and therapies.
Used in Food Industry:
In the food industry, .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)can be used as an additive or ingredient in the development of novel food products. Its unique properties may enhance the taste, texture, or shelf life of certain food items.
Used in Research and Development:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)is used as a research compound for the development of new materials and biological compounds. Its unique structure and properties make it a valuable tool for scientists and researchers working on innovative projects in various fields.
Used in Industrial Applications:
.beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)may also find use in various industrial applications, such as the production of specialty chemicals, materials, or coatings, where its unique properties can be leveraged to create new products or improve existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 102719-11-9 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 102719-11:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*1)=89
89 % 10 = 9
So 102719-11-9 is a valid CAS Registry Number.
102719-11-9Relevant academic research and scientific papers
Preparation of the diastereomerically pure 2S-hydroxy derivative of dihydrolevoglucosenone (cyrene)
Sharipov, Bulat T.,Davydova, Anna N.,Faizullina, Liliya Kh.,Valeev, Farid A.
, p. 200 - 202 (2019/04/25)
Diastereomerically pure levoglucosenone alcohol, synthesized from levoglucosenone, upon hydrogenation on Raney Ni or Pd/BaSO4 undergoes epimerization at C2 atom caused by formation of cyrene by-product and its subsequent non-specific
Synthesis of α-bromoisolevoglucosenone and its cyclopenta annulation
Biktagirov,Faizullina,Salikhov,Safarov,Valeev
, p. 1317 - 1322 (2015/01/08)
4,4-Dimethyl-3-nitro-10,11-dioxatricyclo[6.2.1.02,6]undec-5-en-7-one possessing a bicyclic iridoid skeleton was synthesized in two steps from isolevoglucosenone which was obtained in turn from levoglucosenone through 4-benzyloxy-2-tosyloxy deri
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
