4711-06-2

Basic information

• Product Name: (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol
• Synonyms: (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol;(1R)-1-(2-Quinoxalinyl)-D-erythritol;(1R,2S,3R)-1-(2-Quinoxalinyl)-1,2,3,4-butanetetrol;(1R,2S,3R)-1-(Quinoxaline-2-yl)butane-1,2,3,4-tetrol;Zinc04205660;Zinc04205662
• CAS NO: 4711-06-2
• Molecular Formula: C₁₂H₁₄N₂O₄
• Molecular Weight: 250.25056
• Mol File: 4711-06-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 575.4°C at 760 mmHg
• Flash Point: 301.8°C
• Appearance: /
• Density: 1.495g/cm³
• Vapor Pressure: 4.42E-14mmHg at 25°C
• Refractive Index: 1.706
• Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
• Solubility: DMSO (Slightly), Methanol (Slightly), Pyridine (Slightly)
• CAS DataBase Reference: (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol(4711-06-2)
• EPA Substance Registry System: (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol(4711-06-2)

Safety Data

• Hazardous Substances Data: 4711-06-2(Hazardous Substances Data)

Usage

Description

(1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol is a complex organic compound characterized by its unique stereochemistry and quinoxaline ring structure. It is a chiral molecule with specific configurations at the first, second, and third carbon atoms, which play a crucial role in its properties and potential applications.

Uses

Used in Pharmaceutical Industry:
(1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol is used as an intermediate in the synthesis of 2-Quinoxalinecarboxylic Acid (Q765265), which is a residue of Carbadox (C175825). Carbadox is an antimicrobial drug used in the veterinary industry for the treatment of bacterial infections in animals. (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol's role in the synthesis of this antimicrobial agent highlights its importance in the development of pharmaceuticals for animal health.
Additionally, given its structural features and potential for further chemical modification, (1R,2S,3R)-(2-Quinoxalinyl)-1,2,3,4-butanetetrol may have other applications in the pharmaceutical industry, such as serving as a building block for the development of new drugs with various therapeutic properties. However, further research and development would be required to explore these potential applications fully.

InChI:InChI=1/C12H14N2O4/c15-6-10(16)12(18)11(17)9-5-13-7-3-1-2-4-8(7)14-9/h1-5,10-12,15-18H,6H2/t10-,11-,12+/m1/s1

Upstream product

• 10257-28-0 D-Galactose 
• 95-54-5 1,2-diamino-benzene 
• 50-99-7 D-glucose 
• 657-27-2 L-Lysine hydrochloride 

Downstream Products

• 17460-16-1 1-phenyl-3-(D-erythro-trihydroxypropyl)-1H-pyrazolo[3,4-b]quinoxaline 
• 91-19-0 2,3-diethynylquinoxaline 
• 1593-08-4 Quinoxaline-2-carboxaldehyde 
• 1019-62-1 2-quinoxalin-2-yl-furan-3-ol 
• 494-21-3 2-furan-2-yl-quinoxaline 
• 879-65-2 quinoxaline-2-carboxylic acid 
• 40910-67-6 1-phenyl-1H-pyrazolo<3,4-b>quinoxaline-3-carboxaldehyde 
• 114254-04-5 1-phenyl-1H-pyrazolo[3,4-b]quinoxaline-3-carbaldehyde phenylhydrazone 
• 54571-06-1 quinoxaline-2-carbohydrazide 
• 7065-23-8 ethyl quinoxaline-2-carboxylate 
• 104182-64-1 2-(4-Tolyl-iminomethyl)chinoxalin 
• 62294-76-2 4-quinoxalin-2-ylmethyleneamino-benzoic acid 
• 62294-86-4 4-(quinoxalin-2-ylmethyl-amino)-benzoic acid 
• 269-75-0 1H-Pyrazolo<3.4-b>chinoxalin 

Relevant articles and documents

Degradation of glucose: reinvestigation of reactive α-dicarbonyl compounds

Maillard reactions influence the formation of flavor and color in processed foods in an important way. Reducing sugars and amino acids ultimately react to stable end products. To elucidate the complex formation pathways a vast number of experiments have b

Quinoxalines Derived from D-Glucose and O-Phenylenediamine in Weakly Acidic Medium

-