173467-18-0 Usage
Uses
Used in Organic Synthesis:
METHYL 5,7,8,9-TETRA-O-ACETYL-4-ACYLAMINO-2,6-ANHYDRO-3,4-DIDEOXY-D-GLYCERO-D-GALACTO-2-ENONATE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and functional groups allow for further chemical modifications and reactions, making it a valuable asset in the development of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL 5,7,8,9-TETRA-O-ACETYL-4-ACYLAMINO-2,6-ANHYDRO-3,4-DIDEOXY-D-GLYCERO-D-GALACTO-2-ENONATE is used as a starting material for the development of novel drugs. Its chemical properties and reactivity enable the creation of new drug candidates with potential therapeutic effects, contributing to the advancement of medical treatments.
Used in Chemical Research:
METHYL 5,7,8,9-TETRA-O-ACETYL-4-ACYLAMINO-2,6-ANHYDRO-3,4-DIDEOXY-D-GLYCERO-D-GALACTO-2-ENONATE is also utilized in chemical research to study the properties and behavior of complex organic molecules. Its unique structure provides researchers with valuable insights into the mechanisms of various chemical reactions and interactions, furthering the understanding of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 173467-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,6 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 173467-18:
(8*1)+(7*7)+(6*3)+(5*4)+(4*6)+(3*7)+(2*1)+(1*8)=150
150 % 10 = 0
So 173467-18-0 is a valid CAS Registry Number.
173467-18-0Relevant academic research and scientific papers
Novel practical synthesis of Kdn2en and its C-4 nitrogen-modified derivatives
Sun, Xue-Long,Sato, Noriko,Kai, Toshitsugu,Furuhata, Kimio
, p. 1 - 6 (2007/10/03)
A practical synthesis of Kdn2en and 4-amino-4-deoxy-Kdn2en has been achieved via a key intermediate, methyl 4,5,7,8,9-penta-O-acetyl-2,6-anhydro- 3-deoxy-D-glycero-D-galacto-non-2-enonate, which has been prepared from Kdn in three steps in 91% overall yield. (C) 2000 Elsevier Science Ltd.
Facile synthesis of 4-acylamino-2,6-anhydro-2,3,4-trideoxy-D-glycero-D- galacto-non-2-enoic acids
Sun,Kai,Tanaka,Takayanagi,Furuhata
, p. 1654 - 1658 (2007/10/03)
The title compounds were synthesized from 3-deoxy-D-glycero-D-galacto-2- nonulosonic acid (5, KDN) by a new method which is similar to the Ritter reaction. The structures of these compounds were elucidated from the MS, elemental analysis, 1H-NMR and 13C-NMR data, and the stereochemistry of methyl 4-benzoylamino-5,7,8,9-tetra-O-acetyl-2,6-anhydro-2,3-dideoxy-D- glycero-D-galacto-non-2-enonate (13) was determined by X-ray crystallographic analysis.
