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178915-22-5

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178915-22-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178915-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,9,1 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 178915-22:
(8*1)+(7*7)+(6*8)+(5*9)+(4*1)+(3*5)+(2*2)+(1*2)=175
175 % 10 = 5
So 178915-22-5 is a valid CAS Registry Number.

178915-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,9-dimethylxanthene-4,5-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 9,9-dimethyl-9H-xanthene-4,5-dicarboxylic acid

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:178915-22-5 SDS

178915-22-5Relevant articles and documents

Photoinduced hinge-like molecular motion: Studies on xanthene-based cyclic azobenzene dimers

Nagamani, S. Anitha,Norikane, Yasuo,Tamaoki, Nobuyuki

, p. 9304 - 9313 (2007/10/03)

Molecular devices incorporating azobenzene units represent active components of smart systems, as they are capable of exhibiting photoregulated cooperative molecular motion. Herein, we describe the synthesis, X-ray crystal analysis, and photochemical and thermal studies of a xanthene based cyclic azobenzene dimer and its precursor. The trans-trans isomer of the azobenzene dimer upon photoirradiation transforms to the eis-eis isomer through an intermediate trans-cis isomer. The X-ray crystal structures of the trans-trans isomer (open) and the cis-cis isomer (closed) provide unambiguous proof for the hinge-like molecular motion in this class of molecules. The inferences drawn from photochemical and thermal studies shed light on the effect of varied substitution and cyclic structures on the different transitions. The lifetime of the cis-cis isomer is estimated to be 6.43 years, whereas the trans-cis isomer is short-lived (2.73 min) at 303 K. A rational explanation for the relative stability of the different isomers is derived from the isokinetic plot and theoretical calculations.

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