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Methyl 4-hexyloxybenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50822-54-3

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50822-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50822-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,2 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50822-54:
(7*5)+(6*0)+(5*8)+(4*2)+(3*2)+(2*5)+(1*4)=103
103 % 10 = 3
So 50822-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O3/c1-3-4-5-6-11-17-13-9-7-12(8-10-13)14(15)16-2/h7-10H,3-6,11H2,1-2H3

50822-54-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-hexoxybenzoate

1.2 Other means of identification

Product number -
Other names methyl 4-(hexyloxy)benzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50822-54-3 SDS

50822-54-3Relevant academic research and scientific papers

Naphthoyl hydrazine organic gel factor as well as preparation method and application thereof

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Paragraph 0053-0056, (2021/11/06)

The invention relates to a naphthoyl hydrazine organic gel factor and a preparation method and application thereof. Where n is-18; wherein n is-18. The alkoxy benzoic acid and the condensation agent are mixed into a mixed solution, naphthalene carbonylhydrazide is added and the condensation reaction is carried out, and the alkoxy benzoic acid and the condensation agent are subjected to condensation reaction and can be prepared by separation and purification. The organic gel factor is mixed with an organic solvent, is heated and dissolved in a sealed state, and after cooling, an organic gel with fluorine ion responsiveness can be obtained. Compared with the prior art, the preparation method has the advantages of simple preparation process, mild reaction conditions, good gel ability for various organic solvents such as methanol and ethanol, and the like. The fluorinion has a remarkable specific response to fluoride ions in a gel state, and shows a remarkable advantage in the aspect of fluorine ion detection.

Coupling of Alternating Current to Transition-Metal Catalysis: Examples of Nickel-Catalyzed Cross-Coupling

Bortnikov, Evgeniy O.,Semenov, Sergey N.

supporting information, p. 782 - 793 (2020/12/01)

The coupling of transition-metal to photoredox catalytic cycles through single-electron transfer steps has become a powerful tool in the development of catalytic processes. In this work, we demonstrated that transition-metal catalysis can be coupled to al

“Effect of the linking unit on the calamitic-shaped liquid crystal: a comparative study of two homologous series of benzoate and cinnamate linked compounds”

Kashyap, Dinesh,Patel, Sunil,Prajapat, Varsha,Sharma, Vinay,Vasava, Dilip

, p. 58 - 70 (2019/08/28)

Two homologous series based on three linking groups have been synthesized and well characterized by elemental analyses and spectroscopic techniques such as Fourier transform infrared [FT-IR] and proton magnetic resonance magnetic resonance [1H NMR] spectroscopy. The mesomorphic properties of these compounds were observed by using optical polarized microscopy (POM) and confirmed by differential scanning calorimetry (DSC) analysis. In this present investigation, we have synthesized two homologous series viz. (E)-4-(3-(4-(tetra decanoyloxy) phenyl) acryloyl) phenyl-4-n-alkoxy benzoate (Series-1) and 4-((E)-3-(4-(((E)-3-(4-n-alkoxy phenyl) acryloyl) oxy) phenyl)-3-oxo prop-1-en-1-yl) phenyl tetradecanoate (Series-2). Both of the series are differing with respect to the first linking group. All the homologous in following series displays LC properties on heating as well as cooling condition except first four homologous (C1 to C4) in series-1 and six homologous (C1 to C6) in series-2. To get more insights, the HOMO, LUMO studies are carried out which supports intramolecular charge transfer interactions in this class of mesogens.

“Synthesis, Mesomorphic and DFT Studies of Chalcone Derived Room Temperature Liquid Crystal with Presence of Lateral Nitro and N, N-Dimethyl Amino Terminal Group”

Shukla, Devendra K.,Sharma, Vinay S.,Prajapat, Varsha,Patel

, p. 8 - 26 (2019/10/14)

In this present article, we wish to report on the liquid-crystalline properties of chalcone-ester based homologous series of compounds having aliphatic chain length in n-alkoxy group (n = 1 to 10, 12, 14, 16, 18). The present series consisted thirteen compounds, in which comp.C1 and C2 shows nonliquid crystalline properties, while comp.C3 to C7 display SmC phase and comp.C8 to C18 exhibits only nematic phase. Textural pattern of presently synthesized compounds are schlieren and threaded type. All this compounds were well characterized by elemental analysis, FT-IR and 1H NMR. Phase transition temperatures of present synthesised compounds were determined by optical polarising microscopy (POM), differential scanning calorimetric (DSC). Detailed XRD investigation endorses the presence of the nematic phase in higher homologues and SmC phase in lower homologues. It is shown that chalcone with ester as linking unit favors a calamitic liquid crystalline behaviour in molecules. To get more insights, the DFT based HOMO, LUMO studies are carried out which supports intramolecular charge transfer interactions in this class of mesogens. Chalconyl ester based compounds C3 to C12 shows antibacterial as well as antifungal activity compared with corresponding standard drugs.

Semiheterogeneous Dual Nickel/Photocatalytic (Thio)etherification Using Carbon Nitrides

Cavedon, Cristian,Madani, Amiera,Seeberger, Peter H.,Pieber, Bartholom?us

supporting information, p. 5331 - 5334 (2019/07/08)

A carbon nitride material can be combined with homogeneous nickel catalysts for light-mediated cross-couplings of aryl bromides with alcohols under mild conditions. The metal-free heterogeneous semiconductor is fully recyclable and couples a broad range of electron-poor aryl bromides with primary and secondary alcohols as well as water. The application for intramolecular reactions and the synthesis of active pharmaceutical ingredients was demonstrated. The catalytic protocol is applicable for the coupling of aryl iodides with thiols as well.

1-substituted benzoyl-4-fatty acyl semicarbazide derivative, preparation method and application thereof as antibacterial agent

-

Paragraph 0138-0140, (2018/09/14)

The invention belongs to the technical field of antibacterial agents, and relates to a 1-substituted benzoyl-4-fatty acyl semicarbazide derivative, a preparation method and application thereof as an antibacterial agent. The compound is shown in a formula

Synthesis, characterization, crystal structure and liquid crystal studies of some symmetric naphthalene derivative molecules

Srinivasa,Palakshamurthy,Devarajegowda,Hariprasad

, p. 620 - 626 (2018/09/18)

The synthesis of a series of symmetrical liquid crystals having naphthalene as the central rigid core and attached to long chain flexible 4′-alkoxybenzoate moiety at positions 2,6 - of the aromatic ring are reported. The mesophase behavior of the molecules was investigated using differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-ray diffraction studies. The studies reveal that the synthesized compounds exhibit stable enantiotropic mesophase of Smectic A (SmA) and Nematic (N) phase. The mesophase appearance is independent of the length of the alkyl chain. The molecular structure was determined by single crystal X-ray diffraction technique. The derivative with n-heptyloxy- flexible chain crystallizes under triclinic, P1ˉspace group with unit cell dimension a = 5.569(3) ? b = 10.540(5) ? c = 15.254(9) ? α = 73.434(18)o, β = 80.807(19)o and γ = 82.02(2)o, V = 843.1(8) ?3. The dihedral angle between the naphthalene ring system and the benzoate moiety is 63.63(2)o.

New chalcone based liquid crystals with allylidene amino linking unit: Synthesis and characterization

Sharma, Vinay S.,Sharma, Anuj S.,Jadeja, Upendra H.,Suthar, Deepak

, p. 64 - 81 (2019/02/24)

In this study, the synthesis, structural characterization and mesomorphic properties of newly thirteen calamitic shaped compounds derived from allylidene amino chalcone and 4-n-alkoxy benzoyloxy benzoic acid. Comp.H1 to H3 exhibited nonliquid crystalline nature, while comp.H4 to comp.H18 displayed enantiotropical smectic C phase. Phase transition temperatures of present synthesised compounds were determined by optical polarising microscopy (POM), differential scanning calorimetric (DSC) and powder X-ray diffraction (PXRD) techniques. Thermal stabilities of smectic to isotropic phase are 150.0 °C and temperature range of mesophase is in decreasing order from comp.H3 to comp.H18 respectively. The presences of SmC phase are the type of broken fan and needle type in present synthesized series. It is also shown that presence of chalcone amino allylidene central linking group favors a calamitic liquid crystalline behaviour in molecules with lower member to higher member aliphatic side chain in alkoxy group (-OR).

λ-Shaped mesogens based on chalconyl ester core having variable side chain: Synthesis and characterisation

Sharma, Vinay S.,Suthar, Deepak,Sharma, Anuj S.

, p. 100 - 118 (2019/02/24)

In present study, we have synthesized two newly chalconyl-ester core LCs having variable side chain and fixed disubstituted butoxy group at another terminal end. All this compounds were well characterized by elemental analysis, FT-IR, 1H NMR. The mesomorphic properties of these compounds were observed by optical polarized light microscopy (POM) and also confirmed by using differential scanning calorimetry (DSC) and X-ray diffraction pattern (XRD). Detailed XRD investigation endorses the presence of the nematic phase in higher angle region and SmC phase in lower angle region. In addition, it is found that all the prepared materials display enantiotropic LCs phases except first four members in series-1 and first member in series-2. Thermal stability of SmC and nematic phase of series-1 is higher as compare to series-2. To get more insights, the DFT based HOMO, LUMO studies are carried out which supports intramolecular charge transfer interactions and stability in this class of mesogens.

Calamitic-rod-shaped mesogens based on chalcone esters comprising varying alkoxy and lauryl ester chains: Synthesis, mesomorphism and computational study

Sharma, Vinay S.,Patel, Sunil B.,Sharma, Anuj S.,Patel

, p. 32 - 47 (2017/12/26)

In this studywe have synthesized a new class of compounds incorporating of chalconyl-ester and terminally substituted lauryl group. A series of new chalcones with three aromatic rings is synthesized and characterised by elemental analyses and spectroscopic techniques such as Fourier transform infrared [FT-IR] and proton magnetic resonance magnetic resonance [1H NMR] spectroscopy. The mesomorphic properties of these compounds were observed by optical polarized light microscopy (POM) and confirmed by differential scanning calorimetry (DSC). It is found that all the prepared materials display enantiotropic LCs phases except first two homologue in present series. The lowermember comp. (C3 to C6) display only SmC phase while comp. (C7 to C12) shows smectic C as well as nematic phase. The higher member comp. (C14 to C18) display only nematic phase in heating and cooling condition. To get more insights, the HOMO, LUMO studies are carried out which supports intramolecular charge transfer interactions in this class of mesogens. (Figure presented.).

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