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27980-45-6

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27980-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27980-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,8 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27980-45:
(7*2)+(6*7)+(5*9)+(4*8)+(3*0)+(2*4)+(1*5)=146
146 % 10 = 6
So 27980-45-6 is a valid CAS Registry Number.

27980-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-nitrobenzylidene)-5H-dibenzo[a,d]cycloheptene

1.2 Other means of identification

Product number -
Other names 5-(4-Nitrobenzylidene)-5H-dibenzo[a,d]cycloheptene

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:27980-45-6 SDS

27980-45-6Downstream Products

27980-45-6Relevant articles and documents

Fulvenyl-Functionalized Polyisocyanides: Cross-Conjugated Electrochromic Polymers with Variable Optical and Electrochemical Properties

Schraff, Sandra,Sun, Yu,Pammer, Frank

, p. 5323 - 5335 (2018/08/03)

We describe the preparation of arylisocyanide monomers bearing conjugated fulvenyl groups derived from 9-benzylidene-9H-fluorene (Flu), 5-benzylidene-1,2,3,4-tetraphenylcyclopentadiene (TPCp), and 5-benzylidene-5H-dibenzo[a,d]cycloheptene (Dbs). The electrochemical and optical properties of the monomers and their precursors have been characterized and consistently showed the effect of the conjugation of the respective functional group (-NO2, -NH2, -NHCHO, and N-C) with the fulvenyl moiety. The isocyanides have been subsequently polymerized to the corresponding polyisocyanides (PICs), which exhibited number-average molecular weights of 124-136 kDa (PDI = 2.0-2.7), as determined by gel permeation chromatography in THF vs polystyrene standards. The thermal, optical, and electrochemical properties of the polymers have been studied in detail. Spectroelectrochemical analyses of polymers equipped with redox-active pentafulvene groups show reversible electrochromism, which allows to lower the optical gap from 2.38 to 1.20 eV (Flu) and from 2.27 to 1.55 eV (TPCp) via chemical or electrochemical reduction.

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