4746-18-3

Basic information

• Product Name: 2-(hydroxymethyl)-6-[(6Z)-2,3,4-trihydroxy-5,6-bis(phenylhydrazinylide ne)hexoxy]oxane-3,4,5-triol
• Synonyms: 2-(hydroxymethyl)-6-[(6Z)-2,3,4-trihydroxy-5,6-bis(phenylhydrazinylide ne)hexoxy]oxane-3,4,5-triol
• CAS NO: 4746-18-3
• Molecular Formula: C₂₄H₃₂N₄O₉
• Molecular Weight: 520.5323
• Mol File: 4746-18-3.mol

Chemical Properties

• Boiling Point: 843.8°Cat760mmHg
• Flash Point: 464.1°C
• Appearance: /
• Density: 1.5g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 2-(hydroxymethyl)-6-[(6Z)-2,3,4-trihydroxy-5,6-bis(phenylhydrazinylide ne)hexoxy]oxane-3,4,5-triol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(hydroxymethyl)-6-[(6Z)-2,3,4-trihydroxy-5,6-bis(phenylhydrazinylide ne)hexoxy]oxane-3,4,5-triol(4746-18-3)
• EPA Substance Registry System: 2-(hydroxymethyl)-6-[(6Z)-2,3,4-trihydroxy-5,6-bis(phenylhydrazinylide ne)hexoxy]oxane-3,4,5-triol(4746-18-3)

Safety Data

• Hazardous Substances Data: 4746-18-3(Hazardous Substances Data)

Usage

Molecular structure

Long and complex, consisting of multiple rings and functional groups.

Functional groups

Contains multiple hydroxyl (OH) groups, a hydrazine group, and an oxane core.

Reactivity

Potential reactivity due to the presence of hydroxyl and hydrazine groups.

Biological processes

Involvement in various biological processes due to its functional groups.

Medicinal chemistry applications

Possible use in the development of new drugs or therapeutic agents.

Material development

Potential use in the creation of new materials and bioconjugates.

Biochemical and pharmacological implications

The complex structure and functional groups may have significant effects on biochemical and pharmacological properties.

Research interest

The compound is an interesting subject for further research and exploration due to its unique structure and potential applications.

InChI:InChI=1/C24H32N4O9/c29-12-18-21(33)22(34)23(35)24(37-18)36-13-17(30)20(32)19(31)16(28-27-15-9-5-2-6-10-15)11-25-26-14-7-3-1-4-8-14/h1-11,17-24,26-27,29-35H,12-13H2/b25-11+,28-16u

Upstream product

• 5077-31-6 6-O-β-galactopyranosyl-D-galactose 
• 5239-08-7 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1-> 6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 59-88-1 phenylhydrazine hydrochloride 
• 100-63-0 phenylhydrazine 
• 499-40-1 α-(1,6)-mannobiose 
• 69685-27-4 1,2,3,4-tetra-O-acetyl-6-O-(tetra-O-acetyl-α-D-mannopyranosyl)-β-D-mannopyranose 
• 28154-37-2 1,2,3,4-tetra-O-acetyl-β-D-mannopyranose 
• 13242-53-0 acetobromomannose 
• 83-87-4 β-D-mannopyranose pentaacetate 
• 497-84-7 Isomaltulose 

Downstream Products

• 35426-99-4 D-(1R)-O⁴-β-D-glucopyranosyl-1-(2-phenyl-2H-[1,2,3]triazol-4-yl)-erythritol 
• 35426-99-4 D-(1R)-O⁴-α-D-glucopyranosyl-1-(2-phenyl-2H-[1,2,3]triazol-4-yl)-erythritol 
• 35426-99-4 L_r-3c_F-α-D-galactopyranosyloxy-4cat_F-4-(2-phenyl-2H-[1,2,3]triazol-4-yl)-butane-1,2r_F,4t_F-triol 
• 3082-94-8 Acetic acid (2S,3R,4S,5R,6R)-3,5-diacetoxy-2-{(S)-2-acetoxy-2-[5-(acetyl-phenyl-hydrazonomethyl)-2-phenyl-2H-pyrazol-3-yl]-ethoxy}-6-acetoxymethyl-tetrahydro-pyran-4-yl ester 
• 361389-99-3 6,7-dichloro-2-[(1'R,2'S,3'R)-40-(α-D-glucopyranosyloxy)-1',2',3'-trihydroxybutyl]quinoxaline 

Relevant articles and documents

Hydrophilically functionalized pyrazoles from sugars

An effective and convenient protocol has been developed for the conversion of D-glucose and 6-O-α-D-glucopyranosyl-D-fructose (palatinose, isomaltulose) into 5-[(1'S)-1','2/-dihydroxyethyl]-1-phenylpyrazole-3-carboxaldehyde (4) and 5-[(1'S)-2-(α-D-glucopyranosyloxy)-1-hydroxethyl])-1-phenylpyrazole-3 -carboxaldehyde (5), key steps being the acetic anhydride-promoted dehydrative cyclization of the respective phenylosazones, and subsequent liberation of the N-acetylphenylhydrazone-blocked aldehyde function. Exploitation of the ensuing chemistry of 4 and 5 led to a variety of pyrazole building blocks with a diverse level of hydrophilic substituents (hydroxymethyl, dihydroxyethyl or glucosyl residues) and useful functional groups, such as chloro, cyano, aminomethyl, vinyl and acryloyl moieties.