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Benzenamine, 4-nitro-2-(4-pentyn-1-yloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

917501-64-5

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917501-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917501-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,5,0 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 917501-64:
(8*9)+(7*1)+(6*7)+(5*5)+(4*0)+(3*1)+(2*6)+(1*4)=165
165 % 10 = 5
So 917501-64-5 is a valid CAS Registry Number.

917501-64-5SDS

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 4-nitro-2-pent-4-ynoxyaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-nitro-2-(4-pentyn-1-yloxy)

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:917501-64-5 SDS

917501-64-5Relevant academic research and scientific papers

Photo-crosslinkable second order nonlinear AB2-type monomers: Convenient synthesis and enhanced NLO thermostability

Cheng, Ziyao,Deng, Xiaocong,Li, Qianqian,Li, Zhen,Wang, Ruifang,Zhao, Wenjing

, p. 6380 - 6387 (2020)

In this article, two AB2-type second-order nonlinear optical monomers (DN-SH and DS-SH) containing two double bonds and one thiol group, respectively, were synthesized successfully. These two monomers could be in situ photo-crosslinked via a th

An attempt to modify nonlinear optical effects of polyurethanes by adjusting the structure of the chromophore moieties at the molecular level using "click" chemistry

Li, Zhong'an,Zeng, Qi,Li, Zhen,Dong, Shoucheng,Zhu, Zhichao,Li, Qianqian,Ye, Cheng,Di, Chong'an,Liu, Yunqi,Qin, Jingui

, p. 8544 - 8546 (2007/10/03)

The modification of the nonlinear optical effects (NLO) properties of polyurethanes by adjusting the structure of chromophore moieties at the molecular level by introducing different size of isolation spacers, was illustrated. One of the major problems arising while optimizing organic NLO materials is to efficiently translate the large β values of the organic chromophores into high macroscopic NLO activities of polymers. The isolation parts in the chromophore moieties can weaken the strong intermolecular electrostatic interaction to enhance the resultant macroscopic NLO effect of polymers. The dynamic thermal stabilities of the NLO activities of the polymers are investigated by depoling experiments where the real time decays of their SHG signals are monitored. The results show that the NLO properties do not always increase accompanying with the entanglement of the isolation groups linked to the corresponding chromophore moieties.

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