29836-12-2 Usage
Derivative of d-xylofuranose
A five-membered ring sugar molecule The compound is derived from a sugar molecule with a five-membered ring structure.
Intermediate in synthesis
Used in the synthesis of complex organic molecules 1,2-O-Isopropylidene-5-O-ethoxycarbonyl-d-xylofuranose serves as an intermediate in creating more complex organic compounds, particularly in the production of pharmaceuticals and natural products.
Protective groups
Contains isopropylidene and ethoxycarbonyl groups These groups are commonly used in organic synthesis to protect alcohols and carbohydrates during chemical reactions.
Importance in organic chemistry
Applications in drug and material development The compound is significant in the field of organic chemistry due to its potential use in the development of new drugs and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 29836-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,3 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29836-12:
(7*2)+(6*9)+(5*8)+(4*3)+(3*6)+(2*1)+(1*2)=142
142 % 10 = 2
So 29836-12-2 is a valid CAS Registry Number.
29836-12-2Relevant academic research and scientific papers
Alkyloxycarbonyl group migration in furanosides
Dvorakova, Marcela,Pribylova, Marie,Pohl, Radek,Migaud, Marie E.,Vanek, Tomas
, p. 6701 - 6711 (2012/08/29)
A migration of methyloxycarbonyl group from secondary to primary hydroxyl was observed in furanosides (ribosides and xylosides) under usual desilylation conditions using tetrabutylammonium fluoride. The migration was studied further on several alkyloxycarbonyl furanosides under either basic or acidic conditions. As follows from 13C labelling experiments and product distribution, the migration in xylosides, proceeds intramolecularly via six-membered cyclic carbonate, whereas in ribosides, the migration is intermolecular. Acidic conditions prevented the migration in ribosides whereas the migration in xylosides was circumvented under neutral conditions.
