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(2S,4S,5R,6R)-5-acetamido-4-acetyloxy-2-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid is a complex organic compound with a unique molecular structure. It is characterized by its stereochemistry, with four chiral centers at the 2nd, 4th, 5th, and 6th positions, and the presence of various functional groups such as an acetamido, acetyloxy, hydroxy, and carboxylic acid group. (2S,4S,5R,6R)-5-acetamido-4-acetyloxy-2-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid is a derivative of neuraminic acid, which is a key component of the sialic acid family and plays a crucial role in various biological processes.

16655-75-7

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16655-75-7 Usage

Uses

Used in Pharmaceutical Industry:
(2S,4S,5R,6R)-5-acetamido-4-acetyloxy-2-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid is used as a research compound for studying the inhibition of influenza virus infection. It has been used in guinea pig studies to investigate its potential as an antiviral agent. However, it has been found to be resistant to cleavage by viral sialidase, which may protect it from inactivation and enhance its effectiveness in preventing viral replication.
Used in Drug Development:
(2S,4S,5R,6R)-5-acetamido-4-acetyloxy-2-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid can be used as a starting material or a lead compound in the development of new antiviral drugs. Its unique structure and functional groups can be further modified or optimized to improve its antiviral properties and selectivity. Additionally, it can be used to study the mechanisms of viral entry and replication, which can provide valuable insights for the design of novel therapeutic agents.
Used in Chemical Synthesis:
(2S,4S,5R,6R)-5-acetamido-4-acetyloxy-2-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid can also be used as an intermediate in the synthesis of other complex organic compounds, particularly those with potential pharmaceutical or biological applications. Its versatile structure allows for various chemical reactions and modifications, making it a valuable building block in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 16655-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16655-75:
(7*1)+(6*6)+(5*6)+(4*5)+(3*5)+(2*7)+(1*5)=127
127 % 10 = 7
So 16655-75-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H21NO10/c1-5(16)14-9-8(23-6(2)17)3-13(22,12(20)21)24-11(9)10(19)7(18)4-15/h7-11,15,18-19,22H,3-4H2,1-2H3,(H,14,16)(H,20,21)/t7-,8+,9-,10-,11-,13+/m1/s1

16655-75-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-4-O-acetylneuraminic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:16655-75-7 SDS

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