13036-15-2 Usage
General Description
1,3,4,6-tetra-O-acetylhexopyranose is a chemical compound that is a derivative of hexopyranose, a six-carbon sugar molecule. It is obtained by acetylating all four hydroxyl groups on the hexopyranose ring, resulting in a highly acetylated form of the sugar. 1,3,4,6-tetra-O-acetylhexopyranose is often used in organic synthesis and as a building block for the preparation of other sugar derivatives. Its acetylated form enhances its stability and solubility, making it suitable for various laboratory and industrial applications. Additionally, 1,3,4,6-tetra-O-acetylhexopyranose has been studied for its potential pharmaceutical applications, particularly in the development of new drugs and drug delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 13036-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13036-15:
(7*1)+(6*3)+(5*0)+(4*3)+(3*6)+(2*1)+(1*5)=62
62 % 10 = 2
So 13036-15-2 is a valid CAS Registry Number.
13036-15-2Relevant articles and documents
Glycosyl nitrates in synthesis: Streamlined access to glucopyranose building blocks differentiated at C-2
Wang, Tinghua,Nigudkar, Swati S.,Yasomanee, Jagodige P.,Rath, Nigam P.,Stine, Keith J.,Demchenko, Alexei V.
, p. 3596 - 3604 (2018/05/26)
In an attempt to refine a CAN-mediated synthesis of 1,3,4,6-tetra-O-acetyl-α-d-glucopyranose (2-OH glucose) we unexpectedly discovered that this reaction proceeds via the intermediacy of glycosyl nitrates. Improved mechanistic understanding of this reaction led to the development of a more versatile synthesis of 2-OH glucose from a variety of precursors. Also demonstrated is the conversion of 2-OH glucose into a variety of building blocks differentially protected at C-2, a position that is generally hard to protect regioselectively in the glucopyranose series.
