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39969-30-7

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39969-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39969-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39969-30:
(7*3)+(6*9)+(5*9)+(4*6)+(3*9)+(2*3)+(1*0)=177
177 % 10 = 7
So 39969-30-7 is a valid CAS Registry Number.

39969-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-heptyl-4-[2-(4-heptylphenyl)ethynyl]benzene

1.2 Other means of identification

Product number -
Other names Benzene,1,1'-(1,2-ethynediyl)bis[4-heptyl

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:39969-30-7 SDS

39969-30-7Downstream Products

39969-30-7Relevant articles and documents

Understanding the Polymerization of Diphenylacetylenes with Tantalum(V) Chloride and Cocatalysts: Production of Cyclic Poly(diphenylacetylene)s by Low-Valent Tantalum Species Generated in Situ

Sueyoshi, Shingyo,Taniguchi, Tsuyoshi,Tanaka, Saki,Asakawa, Hitoshi,Nishimura, Tatsuya,Maeda, Katsuhiro

supporting information, p. 16136 - 16146 (2021/09/29)

A systematic investigation of the polymerization of representative diphenylacetylenes with TaCl5and cocatalysts suggested that low-valent Ta species, which are formed by in situ reduction of TaCl5by the cocatalysts, are involved in the polymerization and that the polymerization reaction proceeds by an insertion ring expansion mechanism via the formation of tantalacyclopentadiene intermediates, rather than the previously considered metathesis mechanism. This polymerization mechanism indicates the production of unprecedentedcis-stereoregular cyclic poly(diphenylacetylene)s. Indeed, the possibilities of a cyclic structure and highcis-stereoregularity of the resulting polymers were reasonably supported by the results of their detailed atomic force microscopy (AFM) and NMR analyses, respectively.

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