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Benzaldehyde, 3,4,5-tris(dodecyloxy)-, is a chemical compound characterized by a benzene ring with an aldehyde functional group and three dodecyloxy (C12) groups attached at positions 3, 4, and 5. This structure endows the compound with unique properties, such as solubility in nonpolar solvents and the ability to interact with organic materials, which makes it valuable in various applications.

117241-32-4

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117241-32-4 Usage

Uses

Used in Fragrance and Flavoring Industry:
Benzaldehyde, 3,4,5-tris(dodecyloxy)is utilized as a fragrance and flavoring agent due to its aromatic properties. It contributes to the scent and taste profiles of various consumer products, including perfumes, soaps, and cosmetics, enhancing their appeal to consumers.
Used in Organic Synthesis:
Benzaldehyde, 3,4,5-tris(dodecyloxy)serves as a key intermediate in the synthesis of other organic compounds and materials. Its versatility in chemical reactions makes it instrumental in creating a range of products, from pharmaceuticals to specialty chemicals.
Used in Polymer Chemistry:
Benzaldehyde, 3,4,5-tris(dodecyloxy)finds applications in the field of polymer chemistry, where it is used to develop new polymeric materials with specific properties. The dodecyloxy groups attached to the benzene ring influence the compound's interactions with other organic substances, which is crucial for the design and functionality of polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 117241-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,2,4 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117241-32:
(8*1)+(7*1)+(6*7)+(5*2)+(4*4)+(3*1)+(2*3)+(1*2)=94
94 % 10 = 4
So 117241-32-4 is a valid CAS Registry Number.

117241-32-4Relevant academic research and scientific papers

Co-self-assembled nanoaggregates of BODIPY amphiphiles for dual colour imaging of live cells

Fan, Gang,Lin, Yao-Xin,Yang, Le,Gao, Fu-Ping,Zhao, Ying-Xi,Qiao, Zeng-Ying,Zhao, Qiong,Fan, Yun-Shan,Chen, Zhijian,Wang, Hao

, p. 12447 - 12450 (2015)

Co-self-assembled vesicular nanoparticles of two structurally comparable amphiphilic boron-dipyrromethene (BODIPY) dyes with dequenchable dual colour fluorescence were prepared for ratiometric imaging of live cells.

Phenylene(vinylene) based fluorescent polymer for selective and sensitive detection of nitro-explosive picric acid

Duraimurugan, Kumaraguru,Siva, Ayyanar

, p. 3800 - 3807 (2016)

We report the synthesis of phenylene(vinylene) based blue light emitting polymer by atom transfer radical polymerization with very good yield. Their photophysical properties were studied systematically with increasing polarities of solvent and sensing of nitro aromatics in solution and in vapor phase. The sensory properties of the polymer were studied toward various nitroaromatic compounds like nitrobenzene (NB), nitrotoluene (NT), dinitrobenzene (DNB), dinitrotoluene (DNT), nitro benzoic acid (NBA), 3-nitro benzaldehyde (3-NBA), trinitrotoluene (TNT), 4-nitrophenol (NP), and picric acid (PA) in solution state.

Supramolecular Fluorescent Polymers Containing α-Cyanostilbene-Based Stereoisomers: Z/ E-Isomerization Induced Multiple Reversible Switching

Zhu, Yalan,Zheng, Meiqing,Tu, Yuanyang,Chen, Xiao-Fang

, p. 3487 - 3496 (2018)

Photoresponsive materials play an important role in smart sensors and readable optical devices. The α-cyanostilbene moiety gathers Z/E-isomerization, mesogenic, and aggregation-induced enhanced emission (AIEE) properties together and can be considered as

Piezoflurochromism and Aggregation Induced Emission Properties of 9, 10-bis (trisalkoxystyryl) Anthracene Derivatives

Duraimurugan, Kumaraguru,Sivamani, Jayaraman,Sathiyaraj, Munusamy,Thiagarajan, Viruthachalam,Siva, Ayyanar

, p. 1211 - 1218 (2016)

We report the synthesis of trisalkoxy substituted 9, 10-bis styrylanthracene derivatives (C8-ant and C12-ant) by Heck coupling with very good yield and their photophysical properties. Both C8-ant and C12-ant exhibit aggregation induced emission (AIE), mec

Highly luminescent liquid crystals by connecting 1,3,4-oxadiazole with thiazolo[5,4-d]thiazole units

Bechtold, Ivan H.,Cazati, Thiago,Curcio, Sergio F.,Eccher, Juliana,Falc?o, Eduardo H. L.,Farias, Giliandro,Gallardo, Hugo,Girotto, Edivandro,Malvestiti, Ivani,Manfredi, Alex M.,Salla, Cristian A. M.,Santos, Arthur B. S.,Westphal, Eduard

, (2021)

The direct bonding between a thiazolo[5,4-d]thiazole and two 1,3,4-oxadiazole units allowed us to create a new and versatile rigid core for luminescent liquid crystal, which showed interesting and variable mesomorphic and photophysical properties. From the 5-bis(5-phenyl-1,3,4-oxadiazol-2-yl)thiazolo[5,4-d]thiazole new core, three molecules with different number of alkoxy chains were synthesized and had their properties correlated with the molecular structure. The molecule with two chains showed a smectic C mesophase, while the mesogens with four and six chains presented hexagonal columnar mesomorphism, which was confirmed by POM and XRD measurements. In addition, the molecule with six chains presented liquid crystalline behavior close to room temperature. In solution, the molecules presented strong photoluminescence ranging from blue to yellow, with quantum yields higher than 0.6. Excited state lifetimes allowed to correlate the fluorescence component associated to the different emitting species to the molecular organization in spin coated films. The molecular energy levels, together with thermal stability and possible charge carrier transport due to molecular packing, suggest that these molecules are promising for optoelectronic applications. Overall, this work contributes to the development of the use of thiazolo[5,4-d]thiazole in liquid crystals, demonstrating its great efficiency and versatility.

Fluorescent Columnar Liquid-Crystalline Polymers: Synthesis, Mesomorphic Behaviors and Tunable Emission Wavelengths?

Hao, Xiangnan,Mu, Bin,Tian, Wei,Zhang, Zhelin,Zhao, Yu

, p. 2009 - 2015 (2021)

Fluorescent columnar liquid-crystalline polymers have attracted intensive attention due to their unique features that can be applied in many fields. However, the utilization of molecular engineering to achieve efficient fluorescence tuning has rarely been

Copper and silver nanoparticles stabilized by bistriazole-based dendritic amphiphile micelles for 4-nitrophenol reduction

Patil, Naganath G.,Basutkar, Nitin B.,Ambade, Ashootosh V.

, p. 4546 - 4554 (2017)

Copper and silver nanoparticles were fabricated in aqueous solution using micellar assemblies of dendritic amphiphiles containing triazole rings. Dendritic amphiphiles displaying a bistriazole unit between a hydrophobic benzyl ether dendron and two oligo(

High hole mobility in room temperature discotic liquid crystalline tetrathienoanthracenes

Bala, Indu,De, Joydip,Gupta, Santosh Prasad,Singh, Harpreet,Pandey, Upendra Kumar,Pal, Santanu Kumar

, p. 5629 - 5632 (2020)

Tetrathienoanthracene (TTA), a new discotic core fragment, is explored that shows a remarkably high hole mobility (μh) of 4.22 cm2 V-1 s-1 at room temperature when used in space-charge limited current (SCLC) dev

Perfectly straight nanowires of fullerenes bearing long alkyl chains on graphite

Nakanishi, Takashi,Miyashita, Naoko,Michinobu, Tsuyoshi,Wakayama, Yutaka,Tsuruoka, Tohru,Ariga, Katsuhiko,Kurth, Dirk G.

, p. 6328 - 6329 (2006)

Fullerene derivatives bearing long alkyl chains epitaxially adsorb on the basal plane of graphite forming well-ordered one-dimensional lamellae. Within the lamellae, the C60 moieties are organized in a zigzag-type fashion. The ordering is mainl

Synthesis, characterization and aggregation induced emission properties of anthracene based conjugated molecules

Balasaravanan, Rajendiran,Siva, Ayyanar

, p. 5099 - 5106 (2016)

Aggregation induced emission-active branched and linear 9,10-distyrylanthracene derivatives with different length alkoxy chains have been designed, synthesized and the effect of chain length on the solid-state fluorescence properties systematically investigated. All the three anthracene derivatives possess typical aggregation induced emission (AIE) properties, i.e., they exhibit faint emission in their solutions, but intense emission in their aggregate states, as a result of the dominant nonradiative decay of free intramolecular torsion in the solution and also the restricted torsional motion from supramolecular interaction in the solid states. The results show that these materials exhibit not only AIE properties, but also observed were position and chain length dependent fluorescence properties. The shorter alkoxy chains were more red shifted than the longer ones and also different aggregation behaviours for branched and linear molecules were observed. This work demonstrates once again the accessibility of tuning the solid-state optical properties of organic fluorophores by combining the simple alternation of molecular chemical structures and the physical change of aggregate morphology under external stimuli.

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