3624-30-4

Basic information

• Product Name: (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)
• CAS NO: 3624-30-4
• Molecular Formula: C₁₉H₂₄N₄O₅
• Molecular Weight: 388.4177
• Mol File: 3624-30-4.mol

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)(3624-30-4)
• EPA Substance Registry System: (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(3624-30-4)

Safety Data

• Hazardous Substances Data: 3624-30-4(Hazardous Substances Data)

Usage

Uses

Due to the limited information available on (6E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name), its specific applications are not well defined. However, given its chemical structure, it may have potential uses in various industries such as pharmaceuticals, materials science, or chemical research. It is important to handle this chemical with caution and consult reliable sources for further information on its characteristics and uses.

Upstream product

• 20744-69-8 penta-O-acetyl-L-mannonic acid amide 
• 1195466-89-7 penta-O-acetyl-L-mannonic acid 
• 65944-35-6 Hexa-O-acetyl-keto-L-manno-[2]heptulose 
• 72358-76-0 phenylhydrazine acetate 
• 100-63-0 phenylhydrazine 
• 488-38-0 D-glycero-D-gluco-heptitol 
• 3019-74-7 sedoheptulose 
• 73364-67-7 D-galacto-heptulose phenylosazone 
• 7404-40-2 L-galacto-[2]heptosulose-bis-phenylhydrazone 
• 488-38-0 (2R,3R,4R,5S,6S)-Heptane-1,2,3,4,5,6,7-heptaol 
• 4297-17-0 L-gluco-[2]heptulose 
• 5329-51-1 D-gluco-heptulose phenylosazone 
• 3624-30-4 L-gluco-[2]heptosulose-bis-phenylhydrazone 

Downstream Products

• 100-63-0 phenylhydrazine 
• 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 
• 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-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 
• 74134-91-1 4-(β-D-lyxofuranosyl)-2-phenyl-1,2,3-osotriazole 
• 74134-92-2 4-(α-D-lyxofuranosyl)-2-phenyl-1,2,3-osotriazole 
• 21090-79-9 3,6-anhydro-D-galacto-2-heptulose phenylosazone 
• 21090-79-9 3,6-anhydro-D-talo-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.