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Phenanthrene, 3-(2-phenylethenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41866-97-1

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41866-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41866-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41866-97:
(7*4)+(6*1)+(5*8)+(4*6)+(3*6)+(2*9)+(1*7)=141
141 % 10 = 1
So 41866-97-1 is a valid CAS Registry Number.

41866-97-1SDS

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 cis-3-styrylphenanthrene

1.2 Other means of identification

Product number -
Other names 3-((Z)-Styryl)-phenanthrene

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:41866-97-1 SDS

41866-97-1Downstream Products

41866-97-1Relevant academic research and scientific papers

Role of Charge-Transfer Interactions in Photoreactions. 6. Photoinduced Electron Transfer and Trans -> Cis Isomerization for Styrylphenanthrene-Amine Systems in Acetonitrile

Aloisi, Gian Gaetano,Elisei, Fausto,Goerner, Helmut

, p. 4225 - 4231 (1991)

The decay pathways of the lowest excited singlet state (S1) of trans-n-styrylphenanthrenes (n-StPh, with the location on phenanthrene n = 1, 2, 3, 4, and 9) were studied in acetonitrile at room temperature.Fluorescence lifetimes (τF)

ROLE OF CHARGE-TRANSFER INTERACTIONS IN PHOTOREACTIONS. VIII. FLUORESCENCE QUENCHING AND INDUCTION OF INTERSYSTEM CROSSING AND PHOTOISOMERIZATION BY INORGANIC ANIONS

Aloisi, Gian Gaetano,Elisei, Fausto,Latterini, Loredana,Galiazzo, Guido

, p. 181 - 186 (2007/10/02)

The relevance of intersystem crossing catalysis in the fluorescence quenching of n-styrylphenanthrenes (n-StPh, with n = 1, 2, 3, 9) by iodide, thiocyanate and bromide anions has been investigated.Quenching rate constants (kq) were found to dec

Role of Charge-Transfer Interactions in Photoreactions. 5. Photochemical Behavior of Exciplexes of trans-Styrylphenanthrenes and Amines

Aloisi, G. G.,Elisei, F.

, p. 5813 - 5818 (2007/10/02)

The charge-transfer interactions between the five trans-n-styrylphenanthrene isomers (t-n-StPh, with n = 1, 2, 3, 4, and 9) and amines (tributylamine (TBA), diethylaniline (DEA), and 4-bromodimethylaniline (BrDMA)) have been studied in n-hexane by measuri

Photophysical and Theoretical Studies of Photoisomerism and Rotamerism of trans-Styrylphenanthrenes

Bartocci, G.,Masetti, F.,Mazzucato, U.,Spalletti, A.,Baraldi, I.,Momicchioli, F.

, p. 4733 - 4743 (2007/10/02)

The photophysical and photochemical properties and the ground-state conformational equilibrium of trans-n-styrylphenanthrene (n-StPh, with n = 1, 2, 3, 4, 9) have been studied in inert solvents.The kinetic parameters of the competitive radiative and react

trans --> cis PHOTOISOMERIZATION AND LUMINESCENCE OF THE FIVE ISOMERIC n-STYRYLPHENANTHRENES

Galiazzo, Guido,Spalletti, Anna,Bartocci, Giampiero,Aloisi, Gian Gaetano

, p. 705 - 708 (2007/10/02)

The five isomers of trans-n-styrylphenanthrene (n-StPh, with n = 1, 2, 3, 4, 9) have been prepared by standard procedures.The 4-StPh, not described in the literature, has been spectrally and photochemically characterized.The fluorescence and trans --> cis

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