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59965-20-7

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59965-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59965-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,6 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59965-20:
(7*5)+(6*9)+(5*9)+(4*6)+(3*5)+(2*2)+(1*0)=177
177 % 10 = 7
So 59965-20-7 is a valid CAS Registry Number.

59965-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-3,7-dimethyloctane

1.2 Other means of identification

Product number -
Other names 3,7-dimethyloctyl bromide

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:59965-20-7 SDS

59965-20-7Relevant articles and documents

Large Faraday Rotation in Optical-Quality Phthalocyanine and Porphyrin Thin Films

Nelson, Zachary,Delage-Laurin, Leo,Peeks, Martin D.,Swager, Timothy M.

supporting information, p. 7096 - 7103 (2021/05/29)

The magneto-optical phenomenon known as Faraday rotation involves the rotation of plane-polarized light as it passes through an optical medium in the presence of an external magnetic field oriented parallel to the direction of light propagation. Faraday rotators find applications in optical isolators and magnetic-field imaging technologies. In recent years, organic thin films comprised of polymeric and small-molecule chromophores have demonstrated Verdet constants, which measure the magnitude of rotation at a given magnetic field strength and material thickness, that exceed those found in conventional inorganic crystals. We report herein the thin-film magnetic circular birefringence (MCB) spectra and maximum Verdet constants of several commercially available and newly synthesized phthalocyanine and porphyrin derivatives. Five of these species achieved maximum Verdet constant magnitudes greater than 105 deg T-1 m-1 at wavelengths between 530 and 800 nm. Notably, a newly reported zinc(II) phthalocyanine derivative (ZnPc-OT) reached a Verdet constant of -33 × 104 deg T-1 m-1 at 800 nm, which is among the largest reported for an organic material, especially for an optical-quality thin film. The MCB spectra are consistent with resonance-enhanced Faraday rotation in the region of the Q-band electronic transition common to porphyrin and phthalocyanine derivatives, and the Faraday A-term describes the electronic origin of the magneto-optical activity. Overall, we demonstrate that phthalocyanines and porphyrins are a class of rationally designed magneto-optical materials suitable for applications demanding large Verdet constants and high optical quality.

Extraordinary magnetic field effects on the LC phases of homochiral and racemic 4-cyanoresorcinol-based diamagnetic bent-core mesogens

Ocak, Hale,Bilgin Eran, Belk?z,Nuray, Sevgi,?zkonstanyan, Aykun,Poppe, Silvio,Tschierske, Carsten

, p. 1895 - 1910 (2021/03/01)

4-Cyanoresorcinol based bent-core compounds combining one branched chiral with one achiral linear end-chain have been synthesized in enatiomerically pure and one compound also in racemic form. All homochiral compounds form a chiral cybotactic nematic phase at relatively low temperature with a selective reflection ranging from the near IR to near UV. For the compound with the longest chains superparaelectric and antiferroelectric switching smectic phases were observed, whereas the corresponding racemate is non-polar. This is attributed to sterically induced polarization by the denser packing of uniform enantiomers due to chirality synchronization of the helical conformers. For the racemic mixture this chirality synchronization requires additional surface stabilization. There are unprecedented effects of an applied magnetic field (1 T) on the LC phases, leading to a layer shrinkage by 6-13% for the enantiomer and a layer expansion by 5-8% for the racemate. It is proposed that the magnetic field couples with the π-systems of the almost rod-like molecules. For the racemate this increases the core order, whereas for the enantiomer the reduction of the heliconical twist is considered to provide the major effect. These magnetic field effects could lead to new applications of chiral LC materials at the cross-over between rod-like and bent shapes.

New chemical agents based on adamantane-monoterpene conjugates against orthopoxvirus infections

Agafonov, Alexander P.,Bormotov, Nikolay I.,Korchagina, Dina V.,Maksyutov, Rinat A.,Mozhaytsev, Evgenii S.,Salakhutdinov, Nariman F.,Serova, Olga A.,Shishkina, Larisa N.,Suslov, Evgenii V.,Volcho, Konstantin P.,Yarovaya, Olga I.

, p. 1185 - 1195 (2020/11/03)

Currently, the spectrum of agents against orthopoxviruses, in particular smallpox, is very narrow. Despite the fact that smallpox is well controlled, there is, for many reasons, a real threat of epidemics associated with this or a similar virus. In order to search for new low molecular weight orthopoxvirus inhibitors, a series of amides combining adamantane and monoterpene moieties were synthesized using 1- and 2-adamantanecarboxylic acids as well as myrtenic, citronellic and camphorsulfonic acids as acid components. The produced compounds exhibited high activity against the vaccinia virus (an enveloped virus belonging to the poxvirus family), which was combined with low cytotoxicity. Some compounds had a selectivity index higher than that of the reference drug cidofovir; the highest SI = 1123 was exhibited by 1-adamantanecarboxylic acid amide containing the (-)-10-amino-2-pinene moiety. The produced compounds demonstrated inhibitory activity against other orthopoxviruses: cowpox virus (SI = 30-406) and ectromelia virus (mousepox virus, SI = 39-707). This journal is

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