153666-19-4

• 

• Basic information

  1. Product Name: KETODEOXYNONULOSONIC ACID
  2. Synonyms: Ketodeoxynonulosonic acid (Kdn);Ketodeoxynonulosonic acidfree acid (Kdn)
  3. CAS NO:153666-19-4
  4. Molecular Formula: C9H16O9
  5. Molecular Weight: 268.22
  6. EINECS: N/A
  7. Product Categories: Bioproducts;Sugar derivatives;Carbohydrates & Derivatives
  8. Mol File: 153666-19-4.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: 26-28?C
  2. Boiling Point: 726.8 °C at 760 mmHg
  3. Flash Point: 285.4 °C
  4. Appearance: /
  5. Density: g/cm³
  6. Vapor Pressure: 2.18E-24mmHg at 25°C
  7. Refractive Index: N/A
  8. Storage Temp.: −20°C
  9. Solubility: N/A
  10. PKA: 2.34±0.70(Predicted)
  11. BRN: 5439887
  12. CAS DataBase Reference: KETODEOXYNONULOSONIC ACID(CAS DataBase Reference)
  13. NIST Chemistry Reference: KETODEOXYNONULOSONIC ACID(153666-19-4)
  14. EPA Substance Registry System: KETODEOXYNONULOSONIC ACID(153666-19-4)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: 22-24/25
  4. WGK Germany: 3
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 153666-19-4(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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153666-19-4 Usage

Chemical Properties

White to Off-White Solid

Uses

A naturally occuring deaminated sialic acid, exclusively located at the non-reducing end of the sialyl chains. KDN is a sialic acid derivative with potential for anticancer activity. KDN has also been seen to be in elevated levels in human prostate cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 153666-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,6,6 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153666-19:
(8*1)+(7*5)+(6*3)+(5*6)+(4*6)+(3*6)+(2*1)+(1*9)=144
144 % 10 = 4
So 153666-19-4 is a valid CAS Registry Number.

InChI:InChI=1/C9H16O9/c10-2-4(12)6(14)7-5(13)3(11)1-9(17,18-7)8(15)16/h3-7,10-14,17H,1-2H2,(H,15,16)/p-1/t3-,4+,5+,6-,7-,9-/m0/s1

153666-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	3-Deoxy-D-glycero-D-galacto-2-nonulosonic Acid

1.2 Other means of identification

Product number	-
Other names	2,4,5-trihydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

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	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:153666-19-4 SDS

153666-19-4Upstream product

• 530-26-7 D-Mannose 
• 113-24-6 sodium pyruvate 
• 7306-64-1 2,3,5,6-di-O-isopropylidene-D-mannono-1,4-lactone 
• 1346258-08-9 1-bromo-1,2,3-trideoxy-D-glycero-D-galacto-1-yno-nonitol 
• 64-19-7 acetic acid 
• 1346258-07-8 1-bromo-1,2,3-trideoxy-5,6:8,9-di-O-isopropylidene-D-glycero-D-galacto-1-yno-nonitol 
• 148616-97-1 1,2,3-trideoxy-5,6:8,9-di-O-isopropylidene-D-glycero-D-galacto-1-yno-nonitol 
• 1346258-05-6 1,2,3-trideoxy-5,6;8,9-di-O-isopropylidene-D-manno-non-1-yno-4-ulofuranose 
• 7757-38-2 2,3,5,6-di-O-isopropylidene-D-mannofuranose 

153666-19-4Downstream Products

153666-19-4Relevant articles and documents

Diastereoselective One-Step Synthesis of 2-Keto-3-deoxy-d- glycero-d-galacto-nononic acid (KDN) Analogues as Templates for the Development of Influenza Drugs

Laborda, Pedro,Wang, Su-Yan,Lu, Ai-Min,He, Meng,Duan, Xu-Chu,Qian, Ying-Juan,Jung, Yong-Sam,Liu, Li,Voglmeir, Josef

, p. 3120 - 3125 (2017)

Novel sialic acid scaffolds have great significance in the development of influenza neuraminidase inhibitors. Here the enzymatic synthesis of a wide range of 2-keto-3-deoxy-d-glycero-d-galacto-nononic acid (KDN) analogues via aldol addition of pyruvate to d-mannose, d-glucose, d-galactose, 2-deoxy-d-glucose, d-arabinose, l-arabinose and l-rhamnose using a previously unstudied N-acetylneuraminic acid (Neu5Ac) aldolase derived from the bacterium Dyadobacter fermentas is exemplified. Several of the synthesized KDN analogues showed comparable or better inhibitory activity than unstudied Neu5Ac against the mutated influenza neuraminidases (A/California/04/2009 and A/Anhui/1/2005), which both show resistance to Neu5Ac-based neuraminidase inhibitors, demonstrating that these compounds are promising templates for the development of anti-influenza drugs. (Figure presented.).

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