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9,12-Octadecadienal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26537-70-2

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26537-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26537-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26537-70:
(7*2)+(6*6)+(5*5)+(4*3)+(3*7)+(2*7)+(1*0)=122
122 % 10 = 2
So 26537-70-2 is a valid CAS Registry Number.

26537-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,12-octadecadienal

1.2 Other means of identification

Product number -
Other names 9,12-Octadecadienal

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:26537-70-2 SDS

26537-70-2Relevant academic research and scientific papers

Selective ligand-free cobalt-catalysed reduction of esters to aldehydes or alcohols

Rysak, Vincent,Descamps-Mandine, Armel,Simon, Pardis,Blanchard, Florent,Burylo, Laurence,Trentesaux, Martine,Vandewalle, Maxence,Collière, Vincent,Agbossou-Niedercorn, Francine,Michon, Christophe

, p. 3504 - 3512 (2018/07/29)

Cobalt(ii) salts combined with NaBHEt3 and eventually a base catalyse efficiently and selectively the reduction of esters to aldehydes or alcohols through hydrosilylation by using phenylsilane. Catalyst characterisation by XRD, XPS, TEM and STEM analyses indicates the materials were partially crystalline with the presence of cobalt nanoparticles. Control experiments suggested low valent Co(0) was the active catalytic species involved.

Functionally optimized neuritogenic farinosone C analogs: SAR-study and investigations on their mode of action

Burch, Patrick,Chicca, Andrea,Gertsch, Juerg,Gademann, Karl

supporting information, p. 172 - 177 (2014/03/21)

Several natural products derived from entomopathogenic fungi have been shown to initiate neuronal differentiation in the rat pheochromocytoma PC12 cell line. After the successful completion of the total synthesis program, the reduction of structural complexity while retaining biological activity was targeted. In this study, farinosone C served as a lead structure and inspired the preparation of small molecules with reduced complexity, of which several were able to induce neurite outgrowth. This allowed for the elaboration of a detailed structure-activity relationship. Investigations on the mode of action utilizing a computational similarity ensemble approach suggested the involvement of the endocannabinoid system as potential target for our analogs and also led to the discovery of four potent new endocannabinoid transport inhibitors.

Novel Lipids and Compositions for Intracellular Delivery of Biologically Active Compounds

-

Page/Page column 19, (2012/12/13)

The present invention provides novel amino-lipids, compositions comprising such amino-lipids and methods of producing them. In addition, lipid nanoparticles comprising the novel amino-lipids and a biologically active compound are provided, as well as methods of production and their use for intracellular drug delivery.

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