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26741-30-0

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26741-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26741-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,4 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26741-30:
(7*2)+(6*6)+(5*7)+(4*4)+(3*1)+(2*3)+(1*0)=110
110 % 10 = 0
So 26741-30-0 is a valid CAS Registry Number.

26741-30-0SDS

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 heptadec-2-ene

1.2 Other means of identification

Product number -
Other names 2-Heptadecene

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:26741-30-0 SDS

26741-30-0Downstream Products

26741-30-0Relevant academic research and scientific papers

Selective preparation of terminal alkenes from aliphatic carboxylic acids by a palladium-catalysed decarbonylation-elimination reaction

N?tre, Jér?me Le,Scott, Elinor L.,Franssen, Maurice C. R.,Sanders, Johan P. M.

, p. 3712 - 3715 (2010)

Trialkylamines were used as additives in the decarbonylation-elimination reaction catalysed by the combination of palladium(II) chloride and DPE-Phos. Aliphatic carboxylic acids were transformed at relatively low temperature into terminal alkenes in high yield and high selectivity, without the need for distillation, thereby avoiding isomerisation.

Synthesis and characterization of a supported Pd complex on carbon nanofibers for the selective decarbonylation of stearic acid to 1-heptadecene: The importance of subnanometric Pd dispersion

Bitter, Harry,Fuertes, Sara,Henao, Wilson,Ochoa, Elba,Pinilla, Jose Luis,Scott, Elinor,Suelves, Isabel,Torres, Daniel,Van Haasterecht, Tomas

, p. 2970 - 2985 (2020)

Production of linear α-olefins from renewable sources is gaining increasing attention because it allows the transition from the current petrochemical synthesis route to a more sustainable scenario. In this work, we describe the synthesis and characterization of an innovative catalyst based on a di-μ-chloro-bis[palladium(ii) anthranilate] complex highly dispersed by incipient wetness impregnation over acyl chlorinated carbon nanofibers. The subnanometric dispersion of the metal complex allowed higher catalytic efficiency for the selective decarbonylation of stearic acid to 1-heptadecene as compared to the reference homogenous catalyst. The best catalytic performance (90 mol% selectivity, 71 mol% conversion, and TON = 484) was achieved under mild reaction conditions (atmospheric pressure, 140 °C) with a Pd loading in solution of 0.14 mol%. The post-mortem catalyst characterization and the recyclability tests evidenced the high stability of the catalyst. The highly dispersed catalyst developed in this work provides new opportunities in the rational design of more efficient catalytic systems for the sustainable transformation of fatty acids.

PROCESS FOR PRODUCTION OF OLEFIN

-

, (2011/06/23)

The present invention provides a process for producing an olefin from a carboxylic acid having a β-hydrogen atom or a derivative thereof using the compound containing iodine and at least one metal elements selected from the group consisting of Groups 6, 7, 8, 9, 10 and 11 metals as a catalyst.

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