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cyclohexyl (2E,4E)-hexa-2,4-dienoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16899-71-1

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16899-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16899-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,9 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16899-71:
(7*1)+(6*6)+(5*8)+(4*9)+(3*9)+(2*7)+(1*1)=161
161 % 10 = 1
So 16899-71-1 is a valid CAS Registry Number.

16899-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexyl (2E,4E)-hexa-2,4-dienoate

1.2 Other means of identification

Product number -
Other names Cyclohexyl sorbate

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:16899-71-1 SDS

16899-71-1Downstream Products

16899-71-1Relevant academic research and scientific papers

Ruthenium-Catalyzed Oxidative Cross-Coupling Reaction of Activated Olefins with Vinyl Boronates for the Synthesis of (E, E)-1,3-Dienes

Dethe, Dattatraya H.,Beeralingappa, Nagabhushana C.,Uike, Amar

, p. 3444 - 3455 (2021/02/16)

An oxidative cross-coupling reaction between activated olefins and vinyl boronate derivatives has been developed for the highly stereoselective construction of synthetically useful (E,E)-1,3-dienes. The highlight of this reaction is that exclusive stereoselectivity (only E,E-isomer) was achieved from a base-free, ligand-free, and mild catalytic condition with a less expensive [RuCl2(p-cymene)]2 catalyst.

Polyenic acids. I. Antifungal and bacteriostatic activities of hexa-2,4 dienoic acid derivatives

Le Baut,Sparfel,Clairc,et al.

, p. 441 - 445 (2007/10/02)

Synthesis of esters and amides of 2,4-(2 E, 4 E) hexadienoic acid are reported. The authors have tried to modulate the polarity of these compounds by introducing sequences with hydroxyl, amino groups, ether, thioether functions and halogen atoms or heterocycles. A gain in bacteriostatic activity, compared with sorbic acid has been stated in some cases, it is accompanied by either a breakdown (compounds 3, 38, 51, and 54) or a maintenance of fungistatic activity (compounds 5, 10 and 17).

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