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Benzene,1,4-bis[(10-bromodecyl)oxy]-, also known as 1,4-bis(10-bromodecyl)oxybenzene, is an organic compound with the molecular formula C20H32Br2O2. It is a brominated derivative of benzene, featuring two bromine atoms attached to decyloxy groups that are connected to the benzene ring at the 1,4 positions. Benzene,1,4-bis[(10-bromodecyl)oxy]- is characterized by its symmetrical structure and is often used as an intermediate in the synthesis of various polymers and other chemical products. Due to its bromine content, it may also be relevant in the production of flame-retardant materials. The compound's properties, such as its solubility and reactivity, can be influenced by the presence of the bromine atoms, making it a potentially valuable component in specialized chemical formulations.

6324-68-1

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6324-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6324-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6324-68:
(6*6)+(5*3)+(4*2)+(3*4)+(2*6)+(1*8)=91
91 % 10 = 1
So 6324-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H44Br2O2/c27-21-13-9-5-1-3-7-11-15-23-29-25-17-19-26(20-18-25)30-24-16-12-8-4-2-6-10-14-22-28/h17-20H,1-16,21-24H2

6324-68-1SDS

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-bis(10-bromodecoxy)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:6324-68-1 SDS

6324-68-1Relevant academic research and scientific papers

From bola-amphiphiles to supra-amphiphiles: The transformation from two-dimensional nanosheets into one-dimensional nanofibers with tunable-packing fashion of n-type chromophores

Liu, Kai,Yao, Yuxing,Wang, Chao,Liu, Yu,Li, Zhibo,Zhang, Xi

, p. 8622 - 8628 (2012)

With a rational design of the supra-amphiphiles, we have successfully demonstrated that not only the dimension of the self-assembled nanostructures, but also the packing fashion of the functional naphthalene diimide (a typical n-type chromophore), can be tuned in a noncovalent way in aqueous solution. Naphthalene diimide is incorporated into a bola-amphiphile as the rigid core, whereas viologen derivatives are used as the hydrophilic head. The bola-amphiphile self-assembles into two-dimensional nanosheets, in which naphthalene diimide adopts a "J-type" aggregation. Water-soluble supramolecular complexation between viologen derivatives and the 8-hydroxypyrene-1, 3, 6-trisulfonic acid trisodium salt is used as a driving force for the formation of the supra-amphiphiles. Upon formation of the supra-amphiphiles, the nanosheets transform into ultralong nanofibers with a close packing of naphthalene diimide. Notably, just by mixing the two building blocks of the supra-amphiphiles in aqueous solution, a dimension-controlled evolution of the nanostructures is formed that leads to a different packing fashion of the n-type functional chromophores, which is facile and environmental friendly. Copyright

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