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Disulfide, bis[(4-ethenylphenyl)methyl] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67030-83-5

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67030-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67030-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,3 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67030-83:
(7*6)+(6*7)+(5*0)+(4*3)+(3*0)+(2*8)+(1*3)=115
115 % 10 = 5
So 67030-83-5 is a valid CAS Registry Number.

67030-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-4-[[(4-ethenylphenyl)methyldisulfanyl]methyl]benzene

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:67030-83-5 SDS

67030-83-5Relevant academic research and scientific papers

A Polymerization-Cutting Strategy: Self-Protection Synthesis of Thiol-Based Nanoporous Adsorbents for Efficient Mercury Removal

Xu, Yang,Wang, Tianqi,He, Zidong,Zhou, Minghong,Yu, Wei,Shi, Buyin,Huang, Kun

, p. 14436 - 14441 (2018)

Highly toxic heavy metal ions such as mercury ions (Hg2+) are a great threat to human life and the environment. Developing new strategies and materials to remove the toxic heavy metal ions has attracted more and more attentions. Herein a facile

Reversible crosslinking of polymers bearing pendant or terminal thiol groups prepared by nitroxide-mediated radical polymerization

Braslau, Rebecca,Rivera III, Frank,Tansakul, Chittreeya

, p. 624 - 633 (2013/05/08)

Monomers or N-alkoxyamine initiators containing protected thiol groups are utilized to prepare polymers via nitroxide-mediated radical polymerization. Following thiol deprotection, the macromolecular properties of these polymers are manipulated, by adjusting the redox conditions to either form or cleave disulfide bonds, or irreversibly cap free thiols by the rapid addition to a maleimide Michael acceptor. Formation of disulfide bonds under dilute conditions results in intramolecular disulfide formation, resulting in internal polymer collapse. Alternatively, disulfide formation under high concentration results in intermolecular crosslinking of polymers to form networked macromolecular assemblies.

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