3064-33-3

Basic information

• Product Name: Benzoic acid, 4-(decyloxy)-, hydrazide
• CAS NO: 3064-33-3
• Molecular Formula: C17H28N2O2
• Molecular Weight: 292.422
• Mol File: 3064-33-3.mol

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(decyloxy)-, hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(decyloxy)-, hydrazide(3064-33-3)
• EPA Substance Registry System: Benzoic acid, 4-(decyloxy)-, hydrazide(3064-33-3)

Safety Data

• Hazardous Substances Data: 3064-33-3(Hazardous Substances Data)

Upstream product

• 154845-74-6 4-decyloxy-benzoic acid ethyl ester 
• 62443-10-1 methyl 4-decyloxybenzoate 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 112-29-8 1-bromo dodecane 
• 5519-23-3 p-decyloxybenzoic acid 

Downstream Products

• 1065005-31-3 oxalic acid N',N'-di(4-decyloxybenzoyl)-hydrazide 
• 1630012-61-1 C₂₂H₃₇N₃O₃ 
• 1630013-09-0 4-butyl-5-(4-decyloxyphenyl)-2H-1,2,4-triazole-3(4H)-one 
• 1630012-47-3 C₁₈H₂₆N₂O₃ 
• 339247-23-3 C₂₄H₃₂N₂O₃ 

Relevant articles and documents

Multistability at Room Temperature in a Bent-Shaped Spin-Crossover Complex Decorated with Long Alkyl Chains

An iron(II) pyridyl-benzohydrazonate-based complex decorated with long alkyl chains is reported as a rare spin-crossover compound displaying a wide thermal hysteresis spanning room temperature. On heating, this compound exhibits a spin transition between

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Nonsymmetrical cholesterol dimers constituting regioisomeric oxadiazole and thiadiazole cores: an investigation of the structure-property correlation

Three series of chiral nonsymmetrical dimers were prepared by connecting promesogenic cholesterol to a bent structure derived from a substituted 1,3,4-oxadiazole or 1,2,4-oxadiazole or 1,3,4-thiadiazole moiety. These two mesogenic segments are interconnected through spacers of varying lengths and parity. The structures of the bent achiral unit were systematically varied with different central heterocyclic cores to understand the influence of bent angles on the thermal and gelation behavior. The bent angle of the achiral unit, which is determined by the heterocyclic core, has a major role in the stabilization of frustrated phases. Dimers based on the 1,3,4-oxadiazole unit with a more bent structure stabilized frustrated phases like blue phases and twist grain boundary phases. The bent system with a wider bent angle preferred to stabilize chiral nematic and smectic A phases. It is interesting to note that an increased bent structure reduced the mesophase stability as in the case of dimers based on the 1,3,4-oxadiazole unit, where many compounds exhibited monotropic phases. In the case of dimers with a wider bent angle, enantiotropic mesomorphism was observed. All the compounds showed blue light emission in the solution. Among these chiral dimers, only the compounds based on the 1,3,4-oxadiazole unit showed the gelation ability, which emphasizes how small structural changes like bent angle, dipole moment and the type of heteroatom in the heterocyclic unit affect the macroscopic self-assembly.

Tuning the self-assembly and photophysical properties of bi-1,3,4-thiadiazole derivatives through electron donor-acceptor interactions and their application in OLEDs

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Synthesis and anticonvulsant activity evaluation of 4-butyl-5-(4- alkoxyphenyl)-2H-1,2,4-triazole-3(4H)-ones

A series of 4-butyl-5-(4-alkoxyphenyl)-2H-1,2,4-triazole-3(4H)-ones (6a-6u) was designed and synthesized. The anticonvulsant effects and neurotoxicity of the compounds were evaluated with maximal electroshock test and rotarod test. Among the synthetic compounds, 4-butyl-5-(4-(2-fluorinebenzyl)phenyl)-2H-1,2,4- triazole-3 (4H)-one (6k) was the most potent with ED50 value of 27.4 mg/kg and protective index (PI = TD50/ED50) value of 12.0. Besides the anti-MES efficacy, the potency of compound 6k against seizures induced by pentylenetetrazole (PTZ), 3-mercaptopropionic acid (3-MP), and bicuculline (BIC) was also established, which suggested that the mechanisms of action including enhancing of GABAergic activity might be involved in its anticonvulsant activity.

Synthesis, characterization and mesomorphic investigations of ester-substituted aroylhydrazones possessing a lateral hydroxyl group

The synthesis, characterization and investigation of a new liquid crystalline series of ester containing aroylhydrazones with a lateral hydroxyl group, N-[4-(4′-alkoxy)benzoyloxy-2-hydroxy-benzylidene]-N′- [4″-alkoxybenzoyl]hydrazine (Cm,nLH), with the same or different peripheral alkoxy chains, and some of their nickel(II) and copper(II) complexes are described. All the ligands, except those with no terminal chains on either end of the molecule, exhibit an enantiotropic SmC mesophase, as evidenced by polarizing optical microscopy and differential scanning calorimetric studies. It has been found that addition of a lateral hydroxyl group along with ester-substitution to the aroylhydrazone core increases the mesomorphic as well as thermal stability of the ligands. Also, the coordination of Ni2+ and Cu2+ with the aroylhydraozone core inhibits the mesomorphic potential of the ligands. A temperature dependent Raman study of one of the members, C12,12LH (m = n = 12) has been made to identify phase transitions and to understand the molecular rearrangement as a result of changes in intermolecular interactions at the phase transition. DFT calculations have been performed to obtain the stable electronic structure of the ligand (C6,6LH) and its nickel(II) complex.

Polarization effects in mesogenic isoxazoles and 1,3,4-oxadiazoles

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Liquid crystals derived from semifluorinated alkoxybenzoyl hydrazines

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