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156028-40-9

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156028-40-9 Usage

Family

Brominated phenols

Common uses

a. Production of flame retardants
b. Building block in the synthesis of various organic compounds

Physical state

Colorless to light yellow liquid

Molecular weight

466.23 g/mol

Melting point

-5°C

Solubility

a. High in organic solvents
b. Low in water

Hazard classification

Classified as a hazardous chemical

Potential health risks

a. Skin irritation
b. Eye irritation

Safety precautions

Handle with caution and follow appropriate safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 156028-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,0,2 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156028-40:
(8*1)+(7*5)+(6*6)+(5*0)+(4*2)+(3*8)+(2*4)+(1*0)=119
119 % 10 = 9
So 156028-40-9 is a valid CAS Registry Number.

156028-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dibromo-2,5-dioctoxybenzene

1.2 Other means of identification

Product number -
Other names 2,5-Dioctyloxy-1,4-dibromobenzene

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:156028-40-9 SDS

156028-40-9Relevant articles and documents

Detection of Ethylenediamine Using a Fluorescent Probe in Solution and in a PMMA Matrix

Kim, Yongkyun,Son, Sang-Ho,Lee, Taek Seung

, p. 179 - 188 (2014)

Fluorescent 3′,6′-bis(octyloxy)-p-Terphenyl-4,4′-dialdehyde 3 has been successfully synthesized via a Suzuki cross-coupling reaction of the corresponding dibromo compound with a boronic acid compound in the presence of palladium catalyst. The fluorescent

A Molecular Replication Process Drives Supramolecular Polymerization

Feng, Yuanning,Philp, Douglas

supporting information, p. 17029 - 17039 (2021/10/25)

Supramolecular polymers are materials in which the connections between monomers in the polymer main chain are non-covalent bonds. This area has seen rapid expansion in the last two decades and has been exploited in several applications. However, suitable

A high efficiency pure organic room temperature phosphorescence polymer PPV derivative for OLED

He, Ying,Cheng, Nianhe,Xu, Xin,Fu, Jiawei,Wang, Jun-an

, p. 247 - 251 (2018/11/30)

For the purpose of improving device efficiency and reducing cost, it is necessary to develop pure organic molecules with room temperature phosphorescence (RTP). A high efficiency pure organic RTP polymer, poly-p-phenylene vinylene (PPV) derivative (Br-PPV-CHO), was designed and synthesized, which possesses a blue emission at 496 nm, an emission lifetime of 14.1 μs, and a photoluminescence quantum yield of 12.2%, and the HOMO and LUMO of ?5.35 eV and ?2.75 eV, respectively, showing a great potential application in the emitting layer of OLED. A device fabricated with the PPV derivative as the emitting material layer shows a max luminance of 194 cd/m2 when the Br-PPV-CHO content was 0.5 wt %, demonstrating the best RTP performance. The good properties of Br-PPV-CHO come from the substituent groups of bromine and aromatic aldehyde, and the molecular structure design strategy in the PPV derivative supplies a useful guidance for the design and syntheses of organic RTP materials.

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