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136733-06-7

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136733-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136733-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,3 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136733-06:
(8*1)+(7*3)+(6*6)+(5*7)+(4*3)+(3*3)+(2*0)+(1*6)=127
127 % 10 = 7
So 136733-06-7 is a valid CAS Registry Number.

136733-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-{4-[(E)-Phenyldiazenyl]phenyl}-1H-pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 4-phenylazomaleanil

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:136733-06-7 SDS

136733-06-7Upstream product

136733-06-7Relevant articles and documents

Elucidating the balance between metal ion complexation and polymer conformation in maleimide vinyl ether polymer multilayer structures

Kohli,Rini,Major,Blanchard

, p. 2996 - 3001 (2007/10/03)

We have grown layered assemblies of poly[4-(N-maleimido)azobenzene-co-diisopropyl (2-vinyloxy)-ethylphosphonate], (poly(MAB-VEP)), where interlayer connections are made using zirconium bisphosphonate (ZP) ionic complexation chemistry. The linear optical response of the azobenzene chromophore side group shows constant layer density but a layer-dependent ratio of trans-to-cis isomers. Optical null ellipsometry data show a constant average layer thickness despite the change in conformer ratio. The change in conformer ratio with the growth of multiple polymer layers results from the steric constraints imposed on the polymer side groups by the formation of the ZP interlayer linkage. The driving force for metal ion complexation is greater than the isomerization barrier of S0 azobenzene. Once the layers are formed, the side-groups do not exhibit any changes in conformer ratio, even when exposed to UV for a prolonged period.

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