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Benzoic acid, 4-[[12-[(1-oxo-2-propenyl)oxy]dodecyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112231-57-9

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112231-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112231-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,3 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 112231-57:
(8*1)+(7*1)+(6*2)+(5*2)+(4*3)+(3*1)+(2*5)+(1*7)=69
69 % 10 = 9
So 112231-57-9 is a valid CAS Registry Number.

112231-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(12-prop-2-enoyloxydodecoxy)benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-[[12-[(1-oxo-2-propenyl)oxy]dodecyl]oxy]

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:112231-57-9 SDS

112231-57-9Downstream Products

112231-57-9Relevant academic research and scientific papers

The first blue phase reactive monomers containing a bi-mesogenic core and their side-chain polymers

Wei, Chong-Lun,Lin, Yen-Ting,Chang, Jin-Huai,Chiang, I-Hung,Lin, Hong-Cheu

supporting information, p. 4663 - 4669 (2015/12/05)

Two novel blue phase (BP) reactive monomers M1 and M2 containing a bi-mesogenic core are first reported by introducing two end-attached acrylic spacers with different lengths. Due to the self-assembly of bi-mesogenic cores with the same side-by-side end-attached acrylate spacers in homopolymers P1 and P2, no blue phase could be induced by homopolymerization of M1 and M2. However, by interrupting the self-assembly of bi-mesogenic cores with different side-by-side spacer lengths of copolymers P12, double-twisted cylinders of BPIII could be further extended by copolymerization of M1 and M2 with different molar ratios. With M1:M2 = 5:5 (molar ratio) in both side-chain copolymers P12(soln:5/5) and P12(photo:5/5) rather than binary mixture M1/M2(5/5), the widest BPIII ranges of 5.3 °C and 3.8 °C could be obtained by solution- and photo-polymerization, respectively.

Novel supramolecular side-chain banana-shaped liquid crystalline polymers containing covalent- and hydrogen-bonded bent cores

Wang, Ling-Yung,Tsai, Hsin-Yi,Lin, Hong-Cheu

, p. 1277 - 1288 (2011/10/01)

Novel supramolecular side-chain banana-shaped liquid crystalline (LC) polymer complexes AmBn-N bearing various (m/n) molar ratios of hydrogen- and covalent-bonded bent-core components were acquired by the free radical polymerization, where the hydrogen-bonded (H-bonded) structures were executed via mixing equimolar portions of proton donor (H-donor) polymers AmBn (homopolymers/ copolymers) and pyridyl proton acceptor (H-acceptor) bent cores (small molecules). The influences of the molar ratios of bent-core H-bonded components in side-chain banana-shaped LC polymers and their corresponding polymer complexes on mesomorphic and electro-optical properties were first investigated, The voltage-dependent antiferroelectric properties of spontaneous polarization (Ps) values in the polar smectic phase of the supramolecular side-chain banana-shaped copolymers were also reported. The nematic and tilted smectic phases were verified by XRD measurements, and the SmCP phase was further confirmed by the triangular wave method. Surprisingly, a novel enantiotropic polar smectic (SmCPA) phase was generated in some bent-core side-chain polymer complexes AmBn-N. Therefore, a special approach to constructing (or stabilizing) the SmCP phase was first developed in this study by copolymerization of bent-core covalent- and H-bonded units in side-chain polymer complexes (with proper m/n molar ratios of 16/1 and 10/1) from both bent-core covalent- and H-bonded monomers (i.e., B and A-N units, respectively) without the SmCP phase.

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