102719-11-9 Usage
General Description
".beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)-" is a chemical compound that belongs to the group of hexopyranose molecules. It is a derivative of D-arabinose, which is a common sugar found in various plant sources. .beta.-D-arabino-Hexopyranose, 1,6-anhydro-3-deoxy-4-O-(phenylmethyl)- has a unique structure with an additional phenylmethyl group attached to the 4th carbon atom and a 1,6-anhydro group, which gives it distinct chemical properties. This chemical may have potential applications in the pharmaceutical and food industries, as well as in research and development for new materials and biological compounds. Understanding its structure and properties can lead to potential uses in drug synthesis, food processing, and various industrial applications.
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 articles and documents
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 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