10486-91-6 Usage
Description
2-ACETAMIDO-2-DEOXY-D-GALACTITOL, also known as a 2-deoxyhexitol derivative, is a chemical compound derived from galactitol. In this molecule, the 2-hydroxy substituent is replaced by an acetamido group, which gives it unique properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a therapeutic agent for its unique chemical properties and potential to interact with biological systems.
Used in Chemical Research:
In the field of chemical research, 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a research compound for studying the effects of the acetamido group substitution on the properties and reactivity of galactitol derivatives. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a research compound for investigating the influence of acetamido group substitution on galactitol derivatives.
Used in Material Science:
2-ACETAMIDO-2-DEOXY-D-GALACTITOL may also find applications in material science, particularly in the development of novel materials with specific properties due to the presence of the acetamido group. The expression is: 2-ACETAMIDO-2-DEOXY-D-GALACTITOL is used as a building block for the development of new materials with unique properties in material science.
Check Digit Verification of cas no
The CAS Registry Mumber 10486-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10486-91:
(7*1)+(6*0)+(5*4)+(4*8)+(3*6)+(2*9)+(1*1)=96
96 % 10 = 6
So 10486-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO6/c1-4(12)9-5(2-10)7(14)8(15)6(13)3-11/h5-8,10-11,13-15H,2-3H2,1H3,(H,9,12)/t5-,6+,7+,8-/m0/s1
10486-91-6Relevant articles and documents
Perry,Webb
, p. 2481,2483 (1968)
2-Acetamido-2-deoxyaldonolactones from sugar formazans
Zsoldos-Mady, Virag,Pinter, Istvan,Neszmelyi, Andras,Messmer, Andras,Perczel, Andras
, p. 85 - 96 (2007/10/02)
A new approach towards simple aldonic acid derivatives starting from the corresponding aldoses via the 2-acetamido-2-deoxy formazans resulted in the synthesis of 2-acetamido-2-deoxy-D-galactono-1,4-lactone (8), and its 6-deoxy (11) and 6-azido-6-deoxy (14) analogues on treatment with trifluoroacetic acid.The five-membered ring structure of the lactones and that of the intermediate lactone phenylhydrazone (7) was proved by 1H and 13C NMR studies, including deuterium-induced differential isotope shift (DIS) measurements.With sodium borohydride, lactones 8 and 11 were converted into 2-acetamido-2-deoxy-D-galactitol (15) and its 6-deoxy analogue (17), respectively.
A MECHANISTIC CONSIDERATION OF THE HYDRAZINOLYSIS OF 3-O-SUBSTITUTED 2-ACETAMIDO-2-DEOXY-D-HEXOPYRANOSYL AND -D-HEXITOL RESIDUES IN THE ABSENCE AND PRESENCE OF HYDRAZINIUM SULFATE
Inoue, Yasuo,Kitajima, Ken
, p. 342 - 348 (2007/10/02)
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