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Benzoic acid, 4-[[[4-(hexyloxy)phenyl]methylene]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15012-50-7

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15012-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15012-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,1 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15012-50:
(7*1)+(6*5)+(5*0)+(4*1)+(3*2)+(2*5)+(1*0)=57
57 % 10 = 7
So 15012-50-7 is a valid CAS Registry Number.

15012-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-hexoxyphenyl)methylideneamino]benzoic acid

1.2 Other means of identification

Product number -
Other names p-n-Hexyloxybenzyliden-p-aminobenzoesaeure

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:15012-50-7 SDS

15012-50-7Downstream Products

15012-50-7Relevant academic research and scientific papers

Synthesis and mesomorphic properties of quinoline-8-yl-4-((4-n-alkoxy benzylidene) amino) benzoate: The effect of linkage group

Sharma, Vinay. S.,Vekariya, Rajesh H.,Sharma, Anuj. S.,Patel

, p. 99 - 110 (2017/09/25)

A new homologous series viz. quinoline-8-yl-4-((4-n-alkoxy benzylidene) amino) benzoate based on two central linking groups have been designed and characterised by elemental analyses and spectroscopic techniques such as Fourier transform infrared [FT-IR] and protonmagnetic resonance magnetic resonance [1H NMR] spectroscopy. The mesomorphic properties of these compounds were observed by polarizing optical light microscopy (POM) and confirmed by differential scanning calorimetry (DSC). All synthesized compounds displayed LC property except first two homologue. The lower homologues (n = 4 to 8) display SmA and SmC phase while, in higher homologues (n = 10 to 18) SmC and nematic phasewere seen in heating and cooling condition.

The effect of position of tert-butyl tail group on the formation of liquid crystal in Schiff base ester based homologous series

Sharma,Patel

, p. 53 - 65 (2017/07/04)

We report a newly rod like calamatic liquid crystalline materials, which are constructed by the self-organization of a rod-like carboxylic acid derivative based on Schiff base ester as the linking group with tert butyl tail group. A newly series of 4-(tert-butyl) phenyl 4-((4-alkoxybenzylidene) amino) benzoate with different alkyl chain spacer (n = 1 to 8, 10, 12, 14, 16, and 18) were synthesized and their mesomorphic properties were investigated by differential scanning calorimetry and polarized optical microscopy. All homologous in present series displays mesophase in enantiotropically manner. Thermal stability of SmC-SmA is 137.5 °C. All the compounds were characterized by spectroscopic and elemental analysis. The effects of varying left alkyl side spacer on mesomorphism with its structurally related compounds in series have been discussed.

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