5329-51-1

Basic information

• Product Name: (6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)
• CAS NO: 5329-51-1
• Molecular Formula: C₁₉H₂₄N₄O₅
• Molecular Weight: 388.4177
• Mol File: 5329-51-1.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,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: (6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(5329-51-1)
• EPA Substance Registry System: (6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name)(5329-51-1)

Safety Data

• Hazardous Substances Data: 5329-51-1(Hazardous Substances Data)

Usage

Description

(6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is a dihydrazine compound with a heptane backbone and five hydroxyl groups, used in the field of organic chemistry. It has a molecular formula of C21H26N4O5 and a molecular weight of 414.45 g/mol. (6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) may have potential applications in drug design, pharmaceutical research, or as a reagent in various chemical reactions, although further research and studies are needed to determine its specific uses and properties.

Uses

Used in Pharmaceutical Research:
(6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is used as a compound in pharmaceutical research for its potential applications in drug design. Its unique structure with a heptane backbone and multiple hydroxyl groups may offer novel interactions with biological targets, contributing to the development of new therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, (6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is used as a reagent in various chemical reactions. Its dihydrazine nature allows for a range of synthetic applications, potentially leading to the creation of new molecules with diverse properties and functions.
Used in Drug Design:
(6E,7E)-6,7-bis(2-phenylhydrazinylidene)heptane-1,2,3,4,5-pentol (non-preferred name) is used as a building block in drug design due to its structural complexity and the possibility of forming multiple interactions with biological targets. Its potential to be modified and functionalized makes it a valuable candidate for the development of new pharmaceuticals.

Upstream product

• 3019-74-7 sedoheptulose 
• 100-63-0 phenylhydrazine 
• 73364-67-7 D-galacto-heptulose phenylosazone 
• 7404-40-2 L-galacto-[2]heptosulose-bis-phenylhydrazone 
• 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 
• 4297-17-0 L-gluco-[2]heptulose 
• 72358-76-0 phenylhydrazine acetate 
• 1498-42-6 phosphorodichloridous acid ethyl ester 
• 7732-18-5 water 

Downstream Products

• 3624-30-4 DL-gluco-[2]heptosulose-bis-phenylhydrazone 
• 93711-31-0 (1S)-1-(2-phenyl-2H-[1,2,3]triazol-4-yl)-D-arabitol 
• 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.