68044-68-8

Basic information

• Product Name: (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)
• CAS NO: 68044-68-8
• Molecular Formula: C₁₉H₂₄N₄O₅
• Molecular Weight: 388.4177
• Mol File: 68044-68-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 694.808°C at 760 mmHg
• Flash Point: 374.006°C
• Density: 1.355g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.626
• CAS DataBase Reference: (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(68044-68-8)
• EPA Substance Registry System: (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(68044-68-8)

Safety Data

• Hazardous Substances Data: 68044-68-8(Hazardous Substances Data)

Usage

General Description

"(6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)" is a chemical compound composed of a heptane backbone with two phenylhydrazine groups attached at the 6 and 7 positions. It also contains five hydroxyl (OH) groups attached to the carbon atoms 1, 2, 3, 4, and 5. (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is not commonly used and therefore does not have a preferred name. The presence of the phenylhydrazine groups and hydroxyl groups suggests that this compound may have potential applications in organic synthesis or as a reagent in chemical reactions. However, further research is required to determine the specific properties and potential uses of this compound.

Upstream product

• 4297-17-0 L-gluco-[2]heptulose 
• 100-63-0 phenylhydrazine 
• 3019-74-7 sedoheptulose 
• 73364-67-7 D-galacto-heptulose phenylosazone 
• 7404-40-2 L-galacto-[2]heptosulose-bis-phenylhydrazone 
• 5329-51-1 D-gluco-heptulose phenylosazone 
• 3624-30-4 L-gluco-[2]heptosulose-bis-phenylhydrazone 
• 488-38-0 D-glycero-D-gluco-heptitol 
• 488-38-0 (2R,3R,4R,5S,6S)-Heptane-1,2,3,4,5,6,7-heptaol 
• 72358-76-0 phenylhydrazine acetate 

Downstream Products

• 7510-98-7 D-(1S)-1-(2-phenyl-2H-[1,2,3]triazol-4-yl)-xylitol 
• 3624-30-4 DL-gluco-[2]heptosulose-bis-phenylhydrazone 
• 7510-98-7 L-(1R)-1-(2-phenyl-2H-[1,2,3]triazol-4-yl)-xylitol 
• 100-63-0 phenylhydrazine 
• 21090-79-9 3,6-anhydro-D-gluco-hept-2-ulose phenylosazone 
• 21090-79-9 3,6-anhydro-D-manno-hept-2-ulose phenylosazone 
• 81713-49-7 3,7-anhydro-D-gluco-hept-2-ulose phenylosazone 
• 74134-94-4 4-(β-D-arabinofuranosyl)-2-phenyl-1,2,3-osotriazole 
• 74134-95-5 4-α-D-arabinofuranosyl-2-phenyl-1,2,3-osotriazole 
• 81748-29-0 4-β-D-arabinopyranosyl-2-phenyl-1,2,3-osotriazole 
• 81748-28-9 4-(α-D-arabinopyranosyl)-2-phenyl-2H-1,2,3-triazole 
• 21090-79-9 3,6-anhydro-D-allo-2-heptulose phenylosazone 
• 21090-79-9 3,6-anhydro-D-altro-2-heptulose phenylosazone 
• 21090-79-9 3,6-anhydro-D-galacto-2-heptulose phenylosazone 

Relevant articles and documents

STRUCTURE AND ANOMERIC CONFIGURATION OF THE 3,6-ANHYDRO-OSAZONE DERIVATIVES OBTAINED FROM D-altro-2-HEPTULOSE PHENYLOSAZONE

Dehydration of D-altro-2-heptulose phenylosazone with methanolic sulfuric acid afforded two 3,6-anhydro-osazone derivatives (2 and 3).Compound 3 was obtained as the preponderant isomer, with inversion at C-1 (C-3 of the starting osazone), and 2 was obtained without inversion.Refluxing of 3 with copper sulfate afforded the C-nucleoside analog, namely, 2-phenyl-4-β-D-ribofuranosyl-1,2,3-osotriazole (4).Acetylation of 4 afforded the tri-O-acetyl derivative 5.The anomeric configuration was determined by c.d. and n.m.r. spectroscopy.The mass spectra of compounds 2-5 are discussed.