76585-39-2

Basic information

• Product Name: (2R,3R)-2,3-dihydroxybutanedihydrazide
• CAS NO: 76585-39-2
• Molecular Weight: 178.148
• Mol File: 76585-39-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (2R,3R)-2,3-dihydroxybutanedihydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-2,3-dihydroxybutanedihydrazide(76585-39-2)
• EPA Substance Registry System: (2R,3R)-2,3-dihydroxybutanedihydrazide(76585-39-2)

Safety Data

• Hazardous Substances Data: 76585-39-2(Hazardous Substances Data)

Upstream product

• 38115-91-2 (R,R)-(+)-tartaric acid N,N'-dimethyldiamide 
• 608-68-4 dimethyl L-tartrate 
• 87-91-2 diethyl (2R,3R)-tartrate 
• 87-69-4 tartaric acid 
• 408332-88-7 Diethyl tartrate 
• 405897-14-5 dimethyl tartrate 

Downstream Products

• 143729-34-4 tartaric-bis(p-nitrophenyl)hydrazone 
• 957265-46-2 C₂₂H₂₂N₄O₄ 

Relevant articles and documents

Ultra-fast self-healing PVA organogels based on dynamic covalent chemistry for dye selective adsorption

Ultra-fast self-healing organogels based on dynamic covalent chemistry for dye adsorption were prepared from polyvinyl alcohol (PVA), 4-formylphenylboronic acid (FPBA), and tartaric acid dihydrazide (TDH) by an effective in situ reaction approach. The relative xerogels can adsorb methylene blue selectively with high efficiency. The boronate ester bonds and acylhydrazone bonds endow organogels with a very fast self-healing property. What's more, the chirality can be transferred from TDH to the organogels. The organogels obtained from l-TDH and d-TDH show opposite chirality according to the circular dichroism spectra.

Li+-induced selective gelation of discrete homochiral structural isomers derived from l-tartaric acid

Two chiral structural isomers have been synthesized by molecular engineering of l-tartaric acid. In the presence of LiOH isomer 1 forms a thermally stable, fluorescent gel which exhibits interesting nano-cluster morphology, anomalous optical and rheological properties whilst 2 forms a non-fluorescent solution under similar conditions. The current-voltage (I-V) curve followed a non-linear trend, rationally in close proximity to the diode characteristic curve. This journal is the Partner Organisations 2014.

Synthesis of optically active macrolides with hydrazide fragments from tetrahydropyran and L-(+)-tartaric acid derivatives

The synthesis of two potentially useful optically active 23- and 30-membered macrolides containing a 1,2-diol system and dihydrazide fragments was developed starting from tetrahydropyran. It was based on [1+1]-condensation of 7-oxooctyl-7-oxooctanoate and bis(7-oxooctyl)hexanedioate with L-(+)-tartaric acid hydrazide.