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Cyclopentadecene is an organic compound with the molecular formula C15H26, consisting of a cycloalkene structure with 15 carbon atoms. It is a colorless liquid with a strong, pungent odor and is insoluble in water. This chemical is primarily used as an intermediate in the synthesis of various chemicals, such as fragrances, pharmaceuticals, and polymers. Cyclopentadecene is also utilized as a monomer in the production of specialty polymers and copolymers, which have unique properties and applications in various industries. Due to its reactive nature, it is essential to handle cyclopentadecene with proper safety measures to avoid potential health and environmental risks.

6573-72-4

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6573-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6573-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6573-72:
(6*6)+(5*5)+(4*7)+(3*3)+(2*7)+(1*2)=114
114 % 10 = 4
So 6573-72-4 is a valid CAS Registry Number.

6573-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name CYCLOPENTADECENE

1.2 Other means of identification

Product number -
Other names cyclopentadeca-1,5-diyn-3-ene

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:6573-72-4 SDS

6573-72-4Downstream Products

6573-72-4Relevant academic research and scientific papers

Ruthenium-Catalyzed Dehydrogenation Through an Intermolecular Hydrogen Atom Transfer Mechanism

Huang, Lin,Bismuto, Alessandro,Rath, Simon A.,Trapp, Nils,Morandi, Bill

supporting information, p. 7290 - 7296 (2021/03/01)

The direct dehydrogenation of alkanes is among the most efficient ways to access valuable alkene products. Although several catalysts have been designed to promote this transformation, they have unfortunately found limited applications in fine chemical synthesis. Here, we report a conceptually novel strategy for the catalytic, intermolecular dehydrogenation of alkanes using a ruthenium catalyst. The combination of a redox-active ligand and a sterically hindered aryl radical intermediate has unleashed this novel strategy. Importantly, mechanistic investigations have been performed to provide a conceptual framework for the further development of this new catalytic dehydrogenation system.

CIRCULAR ECONOMY METHODS OF PREPARING UNSATURATED COMPOUNDS

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Paragraph 0062, (2018/01/18)

Methods of preparing unsaturated compounds or analogs through dehydrogenation of corresponding saturated compounds and/or hydrogenation of aromatic compounds are disclosed.

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