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1,1':4',1'':4'',1''':4''',1'''':4'''',1''''':4''''',1''''''-Septiphenyl, 2''',5'''-bis(decyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137068-11-2

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137068-11-2 Usage

Molecular structure

Incorporates seven phenyl rings in a septiphenyl backbone

Derivative

A derivative of septiphenyl

Presence of decyloxy groups

Enhances solubility and compatibility with various matrices

Utilization

Used in the manufacturing of industrial and consumer products such as lubricants, plastics, and polymers

Potential applications

Organic electronics and optoelectronics due to its unique molecular structure and properties

Further research

Required to explore its full range of potential uses and impacts

Check Digit Verification of cas no

The CAS Registry Mumber 137068-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,6 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 137068-11:
(8*1)+(7*3)+(6*7)+(5*0)+(4*6)+(3*8)+(2*1)+(1*1)=122
122 % 10 = 2
So 137068-11-2 is a valid CAS Registry Number.

137068-11-2SDS

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 didecyloxy para-polyphenyl heptamer

1.2 Other means of identification

Product number -
Other names 2''',5'''-Bis-decyloxy-[1,4'

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:137068-11-2 SDS

137068-11-2Upstream product

137068-11-2Downstream Products

137068-11-2Relevant academic research and scientific papers

Influence of two-photon absorption on third-order nonlinear optical processes as studied by degenerate four-wave mixing: The study of soluble didecyloxy subsituted polyphenyls

Zhao, Mingtang,Cui, Yiping,Samoc, Marek,Prasad, Paras N.,Unroe, Marilyn R.,Reinhardt, Bruce A.

, p. 3991 - 4001 (2007/10/02)

We have investigated the influence of two-photon absorption on the third-order nonlinear optical properties of model organic molecules using the technique of degenerate four-wave mixing (DFWM).A theoretical formulation developed here shows that the presence of two-photon absorption, which is related to the imaginary part of the third-order susceptibility χ(3), leads to an enhancement of the effective third-order nonlinearity and to the appearance of effects caused by the formation of two-photon generated excited states.The dynamic behavior of the nonlinearity is then governed by the properties of excited molecules.The nonlinear effects also involve contribution which depend on the fifth power of the electric field.We have performed a systematic study of third-order nonlinear optical properties of alkoxy (-C10H21OCH) substituted p-polyphenyl oligomers using the technique of time-resolved degenerate four-wave mixing with subpicosecond pulses at 602 nm.Experimentally determined values of the second-order hyperpolarizability γ for the oligomers increase smoothly from the monomer to the trimer, with a more rapid increase to the pentamer and to the heptamer.In addition, the hyperpolarizabilities for the pentamer and the heptamer appear to be complex.A smooth increase of the γ value is expected from an increase of the ? conjugation from a shorter chain ligomer to a longer chain oligomer.The more rapid increase of the γ value in the pentamer, and especially in the heptamer, however, cannot be explained satisfactorily by only taking into account the ?-conjugation length.Two-photon absorption for the pentamer and the heptamer at the measurement wavelength of 602 nm is suggested to be important as the observed dynamic behavior is satisfactorily explained by the predictions of the theoretical model presented here.It is shown that the effective γ value for a two-photon absorbing material is a function of optical intensity, pulse width, and sample length if one uses the conventional degenerate four-wave mixing description.

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