32934-08-0 Usage
Uses
Used in Organic Synthesis:
Methyl2,3,6-tri-O-acetyl-4-deoxy-4-fluoro-a-D-galactopyranoside is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for selective reactions and modifications, making it a versatile building block for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl2,3,6-tri-O-acetyl-4-deoxy-4-fluoro-a-D-galactopyranoside is used as a starting material for the synthesis of novel drug candidates. Its unique structure and reactivity enable the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
Methyl2,3,6-tri-O-acetyl-4-deoxy-4-fluoro-a-D-galactopyranoside is also used in chemical research to study the properties and reactivity of complex organic molecules. Its unique structure provides insights into the behavior of similar compounds and contributes to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 32934-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32934-08:
(7*3)+(6*2)+(5*9)+(4*3)+(3*4)+(2*0)+(1*8)=110
110 % 10 = 0
So 32934-08-0 is a valid CAS Registry Number.
32934-08-0Relevant articles and documents
Fluorosugar derivatives of macrolides
-
, (2008/06/13)
Macrolides of formula (I) and methods of treatment of resistance to transplantation, fungal infections and autoimmune diseases such as rheumatoid arthritis and psoriasis using said macrolides of formula (I), STR1 wherein n is 1 or 2; A and B are taken together and form =O or A and B are taken separately and are each OH or A is OH and B is H; R1 is a fluoroglycosyl group; R2 is OH or a fluoroglycosyloxy group; and R3 is an alkyl or allyl group.
An improved synthesis of 4-deoxy-4-fluoro-D-galactopyranosyl derivatives
Koch,Chambers
, p. 295 - 299 (2007/10/02)
This note presents an improved synthesis of 4-deoxy-4-fluoro-D-galactopyranosyl derivatives, using a sterically unencumbered acylating agent such as acetyl chloride.