22435-09-2 Usage
Chemical structure
A pentopyranose molecule with all four hydroxyl groups esterified with benzoyl groups.
Origin
Derived from pentopyranose, a five-carbon sugar.
Esterification
The process of attaching benzoyl groups to the hydroxyl groups of pentopyranose to form the compound.
Purpose
To protect the hydroxyl groups and increase the stability of the compound.
Solubility
Limited solubility in common organic solvents.
Usage
Commonly used as a starting material for the synthesis of more complex organic compounds.
Building block
Used for the preparation of carbohydrates and related structures in organic chemistry research.
Reagent
Serves as a reagent in various chemical reactions.
Importance
An important intermediate in organic synthesis with potential applications in academic and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 22435-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,3 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22435-09:
(7*2)+(6*2)+(5*4)+(4*3)+(3*5)+(2*0)+(1*9)=82
82 % 10 = 2
So 22435-09-2 is a valid CAS Registry Number.
22435-09-2Relevant articles and documents
Synthesis of a Tridecasaccharide Lipooligosaccharide Antigen from the Opportunistic Pathogen Mycobacterium kansasii
Bai, Bing,Liu, Yu-Hsuan,Lowary, Todd L.,Shen, Ke
supporting information, p. 24859 - 24863 (2021/10/25)
The outer surfaces of mycobacteria, including the organism that causes tuberculosis, are decorated with an array of immunomodulatory glycans. Among these are lipooligosaccharides (LOSs), a class of molecules for which the function remains poorly understoo
Uncatalyzed and chorismate mutase catalyzed claisen rearrangements of 5,6-dihydrochorismate and 6-Oxa-5,6-dihydrochorismate
Delany III, John J.,Padykula, Robert E.,Berchtold, Glenn A.
, p. 1394 - 1397 (2007/10/02)
The synthesis of 6-oxa-5,6-dihydrochorismic acid (4) from D-xylose is described. The half-lives for the uncatalyzed Claisen rearrangements of 5,6-dihydrochorismic acid (3) and 4 in D2O at 30 °C were 49000 and 1200 h, respectively, compared to a