5934-40-7

Basic information

• Product Name: (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name)
• CAS NO: 5934-40-7
• Molecular Formula: C₁₇H₂₀N₄O₃
• Molecular Weight: 328.3657
• Mol File: 5934-40-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 579.818°C at 760 mmHg
• Flash Point: 304.463°C
• Density: 1.263g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.614
• CAS DataBase Reference: (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name)(5934-40-7)
• EPA Substance Registry System: (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name)(5934-40-7)

Safety Data

• Hazardous Substances Data: 5934-40-7(Hazardous Substances Data)

Usage

Description

(4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name) is a complex organic compound with the molecular formula C17H22N4O3. It features a pentane-1,2,3-triol backbone with multiple hydrazine functional groups attached, indicating a potential for diverse interactions and reactivity in chemical processes.

Uses

Used in Organic Chemistry Research:
(4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name) is used as a research compound for exploring its unique structural properties and reactivity in organic chemistry. Its hydrazine groups and pentane-1,2,3-triol backbone may offer novel pathways for chemical synthesis and reactions.
Used in Biochemistry Applications:
In biochemistry, (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name) may serve as a starting material for the development of new bioactive molecules. Its complex structure could potentially interact with biological systems, providing a basis for the creation of new drugs or diagnostic tools.
Used in Pharmaceutical Research:
(4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name) (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name) is used in pharmaceutical research to investigate its potential as a precursor for medicinal compounds. Its unique structure may lead to the discovery of new therapeutic agents, particularly given the presence of hydrazine groups that are known to be important in certain drug classes.
Given the limited information available about (4E,5E)-4,5-bis(2-phenylhydrazinylidene)pentane-1,2,3-triol (non-preferred name), further research is necessary to fully understand its properties and potential applications across various fields.

Upstream product

• 87-72-9 D-Xylose 
• 100-63-0 phenylhydrazine 
• 58-86-6 D-xylose 
• 65604-80-0 mixture of 3-O-<α-L-rhamnopyranosyl-(1->2)><β-D-xylopyranosyl(1->3)>-β-D-glucopyranosides of diosgenin and yamogenin 

Downstream Products

• 109068-30-6 D-threo-[2]pentosulose-1-(methyl-phenyl-hydrazone)-2-phenylhydrazone 
• 19694-88-3 D-threo-pentos-2-ulose 
• 15476-33-2 2-phenyl-4-(D-threo-1',2',3'-trihydroxypropyl)-2H-1,2,3-triazole 
• 3082-93-7 5-acetoxymethyl-1-phenyl-1H-pyrazole-3-carbaldehyde acetyl-phenyl-hydrazone 
• 6453-44-7 1-phenyl-1H-pyrazole-3,5-dicarboxylic acid 
• 98783-55-2 5-hydroxymethyl-1-phenyl-1H-pyrazole-3-carbaldehyde acetyl-phenyl-hydrazone 
• 148832-76-2 1-phenylpyrazole-3,5-dicarboxaldehyde 
• 211682-80-3 5-Hydroxymethyl-1-phenyl-1H-pyrazole-3-carbaldehyde 
• 211682-77-8 Acetic acid 5-formyl-2-phenyl-2H-pyrazol-3-ylmethyl ester 
• 211682-76-7 [2-Phenyl-5-(phenyl-hydrazonomethyl)-2H-pyrazol-3-yl]-methanol 

Relevant articles and documents

Highly efficient and selective biocatalytic acylation studies on triazolylsugars

Different acid anhydrides (of C2 to C7 aliphatic fatty acids and benzoic acid) have been used to study the selective acylation of primary/secondary hydroxyl groups in 2-phenyl-4-(D-threo-1′,2′, 3′-trihydroxypropyl)-2H-1,2,3-triazole, 2-phenyl-4-(D-erythro-1′, 2′,3′-trihydroxypropyl)-2H-1,2,3-triazole, 2-phenyl-4-(D-arabino- 1′,2′,3′,4′-tetrahydroxybutyl)-2H-1,2,3-triazole and 2-phenyl-4-(D-lyxo-1′,2′,3′,4′-tetrahydroxybutyl)-2H-1, 2,3-triazole in the presence of Candida antarctica lipase B in diisopropyl ether. Among the different acid anhydrides, butanoic anhydride was found to be the most efficient acylating agent (for butanoylation); for acetylation, vinyl acetate gave the best results. The reactions with both these acylating agents were highly selective and efficient yielding exclusively the monoacylated products in 95-99% yields in 1-5 h.

Comparative Studies on the Constituents of Ophiopogonis Tuber and Its Congeners. I. Studies of the Constituents of the Subterranean Part of Liriope platyphylla Wang et Tang.

Eight steroidal glycosides, tentatively named glycosides A(1), B(2), C(3), D(4), E(5), F(6), G(7) and H(8), were isolated from the methanol extract of the subterranean part of Liriope platyphylla Wang et Tang (Liliaceae).The structures of these glycosides were established as ruscogenin 3-O-α-L-rhamnopyranoside (1), 25(S)-ruscogenin 1-O-β-D-fucopyranosido-3-O-α-L-rhamnopyranoside (2), 25(S)-ruscogenin 1-O-α-L-rhamnopyranosyl-(1->2)-β-D-fucopyranoside (3), ruscogenin 3-O-β-D-glucopyranosyl(1->3)-α-L-rhamnopyranoside (4), a mixture of 3-O-2)>3)>-β-D-glucopyranosides of diosgenin and yamogenin (=a mixture of ophiopogonin D' and its 25(S)-isomer, 5), a mixture of 3-O-β-chacotriosides of diosgenin and yamogenin (= a mixture of dioscin and its 25(S)-isomer, 6), ruscogenin 1-sulfate 3-O-α-L-rhamnopyranoside (7), and 26-O-β-D-glucopyranosyl-22-O-methylfurost-5-ene-3β,26-diol 3-O-β-chacotrioside (=methyl proto-dioscin, 8).