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782504-06-7

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782504-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 782504-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,2,5,0 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 782504-06:
(8*7)+(7*8)+(6*2)+(5*5)+(4*0)+(3*4)+(2*0)+(1*6)=167
167 % 10 = 7
So 782504-06-7 is a valid CAS Registry Number.

782504-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,9'-spirobi[fluorene]-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-cyano-9,9'-spirobiflouorene

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:782504-06-7 SDS

782504-06-7Downstream Products

782504-06-7Relevant articles and documents

Synthesis, structures, and photoinduced electron transfer reaction in the 9,9′-spirobifluorene-bridged bipolar systems

Wong, Ken-Tsung,Ku, Sung-Yu,Cheng, Yi-Ming,Lin, Xiauo-Yun,Hung, Ying-Yueh,Pu, Shih-Chieh,Chou, Pi-Tai,Lee, Gene-Hsiang,Peng, Shie-Ming

, p. 456 - 465 (2006)

A series of 9,9′-spirobifluorene-bridged bipolar compounds DnAm bearing various n:m ratios for triarylamine (D) versus 1,3,4-oxadiazole- conjugated oligoaryl moiety (A) have been synthesized to investigate the corresponding photoinduced electron transfer (PET) property. The excitation behaviors were probed by steady-state absorption, emission, fluorescence solvatochromism, and femtosecond fluorescence up-conversion spectroscopy. The overall reaction dynamics can be rationalized by the rate of PET, in combination with solvent relaxation dynamics. It was found that the rate of PET is dependent on the anchored D/A ratio. The rate of D1A1 and D2A1 was resolved to be ~2.44 × 1012 and 2.32 × 1012 s -1, respectively, while it is irresolvable in D1A2 and D2A2 (>6.6 × 1012 s-1). In another approach, based on the comprehensive X-ray data, cyclic voltammetry, and absorption/emission spectra, the rate of photoinduced electron transfer was also qualitatively estimated. Fair comparisons were made between experimental and theoretical approaches to gain detailed insight into the PET for the titled systems.

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