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Benzene, 1-(bromomethyl)-4-(dodecyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123436-89-5

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123436-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123436-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 123436-89:
(8*1)+(7*2)+(6*3)+(5*4)+(4*3)+(3*6)+(2*8)+(1*9)=115
115 % 10 = 5
So 123436-89-5 is a valid CAS Registry Number.

123436-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(bromomethyl)-4-dodecoxybenzene

1.2 Other means of identification

Product number -
Other names 1-(bromomethyl)-4-(dodecyloxy)benzene

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:123436-89-5 SDS

123436-89-5Relevant academic research and scientific papers

New ionic liquid crystals based on imidazolium salts

Dobbs, William,Douce, Laurent,Allouche, Lionel,Louati, Alain,Malbosc, Francois,Welter, Richard

, p. 528 - 532 (2006)

The new ionic liquid crystal 1-(4-dodecyloxybenzyl)-3-methyl-1H-imidazol-3- ium bromide has been synthesized and its X-ray structure obtained; various salts containing BF4-, SCN-, PF6 -, CF3/sub

Microenvironment response type cross-linked quaternary ammonium salt micelle antibacterial agent and preparation method and application thereof

-

Paragraph 0029; 0031; 0043; 0048, (2019/05/23)

The invention discloses a microenvironment response type cross-linked quaternary ammonium salt micelle antibacterial agent and a preparation method and application thereof, and belongs to the field ofbiomedical materials. Crosslinked micelles can well pen

Nanoparticles and nanoparticle compositions

-

Page/Page column 44; 45, (2016/06/01)

The invention provides multivalent surface-crosslinked micelle (SCM) particles, crosslinked reverse micelle (CRM) particles, and methods of making and using them. The SCM particles can be used, for example, to inhibit a virus or bacteria from binding to a host cell. The inhibition can be used in therapy for the flu, cancer, or AIDS. The CRM particles can be used, for example, to prepare metal nanoparticles or metal alloy nanoparticles, or they can be used in catalytic reactions.

Luminescent columnar liquid crystals based on 1,3,4-oxadiazole

Girotto, Edivandro,Eccher, Juliana,Vieira, André A.,Bechtold, Ivan H.,Gallardo, Hugo

, p. 3355 - 3360 (2014/05/06)

In this study five new compounds, derivatives of 1,3,4-oxadiazole, were synthesized in order to achieve mesomorphic behavior and luminescence. Different types of aliphatic chains were used in order to investigate the influence of alkoxide groups in mesomorphic behavior. All of the compounds showed high thermal stability and strong blue photoluminescence in solution and in solid films. Furthermore, compounds 10a-d presented hexagonal columnar mesomorphism, which was characterized by polarizing optical microscopy and X-ray diffraction, and strong π-stacking was observed. Notably, for two compounds (10c,d), the liquid crystal properties were preserved on cooling from the isotropic state to room temperature. These characteristics make these materials good candidates for application in organic electronics.

NANOPARTICLES AND NANOPARTICLE COMPOSITIONS

-

Paragraph 0195; 0196, (2013/05/08)

The invention provides multivalent surface-crosslinked micelle (SCM) particles, crosslinked reverse micelle (CRM) particles, and methods of making and using them. The SCM particles can be used, for example, to inhibit a virus or bacteria from binding to a host cell. The inhibition can be used in therapy for the flu, cancer, or AIDS. The CRM particles can be used, for example, to prepare metal nanoparticles or metal alloy nanoparticles, or they can be used in catalytic reactions.

Artificial light-harvesting system based on multifunctional surface-cross-linked micelles

Peng, Hui-Qing,Chen, Yu-Zhe,Zhao, Yan,Yang, Qing-Zheng,Wu, Li-Zhu,Tung, Chen-Ho,Zhang, Li-Ping,Tong, Qing-Xiao

supporting information; scheme or table, p. 2088 - 2092 (2012/04/18)

A good harvest: Two self-assembling strategies (micellization and electrostatic attraction) and covalent capture were employed to construct a robust, inexpensive, efficient artificial light-harvesting system (see picture). The synthesis was achieved by a one-pot reaction. A high density of the antenna chromophores was achieved without self-quenching and excimer formation, thus affording extremely efficient energy transfer. Copyright

New achiral phenylacetylene monomers having an oligosiloxanyl group most suitable for helix-sense-selective polymerization and for obtaining good optical resolution membrane materials

Liu, Lijia,Zang, Yu,Hadano, Shingo,Aoki, Toshiki,Teraguchi, Masahiro,Kaneko, Takashi,Namikoshi, Takeshi

, p. 9268 - 9276 (2011/11/14)

To develop new phenylacetylene monomers more suitable for helix-sense-selective polymerization (HSSP) we reported previously and to improve the efficiency of the HSSP and membrane performance of the resulting polymers, novel phenylacetylenes having a flexible oligosiloxanyl group (SnBDHPA)together with the other related three series of monomers were synthesized and polymerized by using a chiral catalytic system and enantioselectivity in permeation of the membranes from the resulting chiral polymers were examined. SnBDHPA was the most suitable for the HSSP and the CD absorptions (G values) of poly- (SnBDHPA) were stronger and more stable than those of the corresponding polymers having rigid alkyl groups. The polymers could be fabricated to flexible self-supporting membranes by using solvent-casting method. In addition, enantioselectivity in permeation of one of poly(SnBDHPA) membranes was much higher than that of a poly(phenylacetylene) membrane having alkyl groups. This was because the polymers having oligosiloxane groups had high regularity of structures, i.e., chemical structures of the macromolecules such as one handedness and high order structures such as columnar contents in the membranes, and the membranes were flexible and had almost no defects. These good properties as optical resolution membrane materials were caused by flexibility, hydrophobicity, and bulkiness of the oligosiloxane chains. S3BDHPA having a trisiloxanyl group was found to be the best monomer for the HSSP and for obtaining good optical resolution membrane materials.

Synthesis and helix-sense-selective polymerization of a novel phenylacetylene having a trisiloxanyl group and two hydroxyl groups and enantioselective permeability of the resulting chiral polymeric membrane: Effect of the trisiloxanyl group on the polymerization and enantioselective permeability

Liu, Lijia,Oniyama, Yoshiyuki,Zang, Yu,Hadano, Shingo,Aoki, Toshiki,Teraguchi, Masahiro,Kaneko, Takashi,Namikoshi, Takeshi,Marwanta, Edy

experimental part, p. 2460 - 2464 (2011/11/12)

To develop a new phenylacetylene monomer suitable for helix-sense-selective polymerization (HSSP) we reported previously and to improve the efficiency of the HSSP and membrane performance of the resulting polymer, a novel phenylacetylene having a trisiloxanyl group (S3BDHPA) was synthesized and polymerized by using a chiral catalytic system and enantioselectivity in permeation of its membrane was examined. S3BDHPA was suitable for the HSSP and the CD absorption of poly(S3BDHPA) was stronger and more stable than that of the corresponding polymer having no siloxanyl groups. In addition, enantioselectivity in permeation of poly(S3BDHPA) was much higher than that of a polymer membrane having no siloxanyl groups. They are thought to be caused by the flexibility and hydrophobicity of the trisiloxane groups.

1-(4-Alkyloxybenzyl)-3-methyl-1H-imidazol-3-ium organic backbone: A versatile smectogenic moiety

Dobbs, William,Douce, Laurent,Heinrich, Benoit

experimental part, (2010/04/22)

The merger of ionic liquid and liquid crystal fields, obtained by using the imidazolium ring as a common element, has allowed us to tailor a new set of materials which associate specific functionalities. These functionalities are consequences of the origi

Synthesis of oligo(ethylene glycol) toward 44-mer

Ahmed, Saleh A.,Tanaka, Mutsuo

, p. 9884 - 9886 (2007/10/03)

A synthetic method for oligo(ethylene glycol) toward 44-mer (FW = 1956.35) is described. Reiteration of Williamson's ether synthesis and hydrogenation to remove protecting benzyl group affords desired oligo(ethylene glycol) toward 44-mer in moderate yields. The advantages in this method are use of commercially easily available materials as starting materials and procedures avoiding difficulty in purification of the products as much as possible.

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