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

38454-16-9

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38454-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38454-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,5 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38454-16:
(7*3)+(6*8)+(5*4)+(4*5)+(3*4)+(2*1)+(1*6)=129
129 % 10 = 9
So 38454-16-9 is a valid CAS Registry Number.

38454-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-hexyloxyphenoxy)carbonyl]phenyl 4-hexyloxybenzoate

1.2 Other means of identification

Product number -
Other names -

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:38454-16-9 SDS

38454-16-9Downstream Products

38454-16-9Relevant academic research and scientific papers

Synthesis and mesophase characterization of novel methacrylate based thermotropic liquid crystalline monomers and their polymers

Siva Mohan Reddy,Narasimhaswamy,Mohana Raju

, p. 4357 - 4364 (2014)

A new series of side chain methacrylate monomers with a three phenyl ring core connected by an ester with a terminal alkoxy chain and hexamethylene spacer are synthesized by a multistep synthetic route. The corresponding polymers are realized by free radical solution polymerization. Two structurally similar mesogens are also synthesized for use as models to study the influence of the methacrylic unit on the mesophase characteristics. The molecular structure of the intermediates, monomers as well as the polymers is unambiguously confirmed by Fourier-transform infrared (FT-IR), solution 1H and 13C nuclear magnetic resonance (NMR) spectroscopy and by elemental analysis. The mesophase characteristics of all of the monomers and polymers are determined by hot-stage optical polarized microscopy (HOPM) and differential scanning calorimetry (DSC). These investigations revealed the existence of enantiotropic nematic (N), smectic A (SA) and smectic C (SC) mesophases. Furthermore, for a representative monomer and polymer, the presence of the smectic phase is confirmed by variable temperature X-ray diffraction (XRD) where a characteristic layer ordering is noticed. The molecular weight of the polymers is determined by gel permeation chromatography (GPC) and the values are found to be typically in the range of 2.0 × 103 to 3.7 × 103. The mesogenic polymers are also found to be stable up to 320 °C by thermogravimetric analysis (TGA). the Partner Organisations 2014.

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