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72045-59-1

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72045-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72045-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,4 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72045-59:
(7*7)+(6*2)+(5*0)+(4*4)+(3*5)+(2*5)+(1*9)=111
111 % 10 = 1
So 72045-59-1 is a valid CAS Registry Number.

72045-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(7-diazonioimino-9H-fluoren-2-ylidene)hydrazinylidene]azanide

1.2 Other means of identification

Product number -
Other names 2,7-Diazido-9H-fluorene

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:72045-59-1 SDS

72045-59-1Upstream product

72045-59-1Downstream Products

72045-59-1Relevant articles and documents

Semiconducting polymer thin films by surface-confined stepwise click polymerization

Hwang, Euiyong,Lusker, Kathie L.,Garno, Jayne C.,Losovyj, Yaroslav,Nesterov, Evgueni E.

supporting information; experimental part, p. 11990 - 11992 (2011/12/16)

Surface-confined stepwise click polymerization was used to prepare surface-attached thin films of semiconducting polymers. These highly uniform films showed extended UV/vis absorption characteristics and a remarkable degree of molecular organization with a unidirectional alignment of the polymer chains normal to the surface.

Effects of additional linkers in biphenyl-4,4′-dinitrene on the low-lying singlet-triplet energy gap and zero-field splitting

Nimura,Kikuchi,Ohana,Yabe,Kondo,Kaise

, p. 2083 - 2088 (2007/10/03)

Perturbation effects of additional linkers on the spin-spin coupling in biphenyl-4,4′-dinitrene (1) were examined by introducing a linking group between 2- and 2′-positions of 1. Five different doubly linked systems showed triplet ESR spectra corresponding to quinonoid dinitrenes. Curie law analyses suggested that all those triplet states were thermally excited triplet states. In addition, the singlet-triplet energy gaps, which were determined by the Curie law analyses, were well correlated with their corresponding zero-field-splitting (zfs) D values. The result could be explained by the stability of dinitrene character which is estimated from the resonance energy of the intervening π-system. Our semiempirical molecular orbital calculations supported the experimental correlation between the singlet-triplet energy gap and the zfs D value.

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