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2,4,6,8,10-Undecapentaenoic acid, 5,9-dimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (2E,4E,6E,8E,10E)- is a complex organic compound with a long carbon chain and multiple double bonds. It is characterized by its 11-carbon backbone, with five double bonds (denoted by the E configuration, indicating the trans arrangement of the double bonds) and various methyl groups attached to different carbon atoms. This molecule is a type of fatty acid, which are essential components of cell membranes and play a crucial role in various biological processes. The specific structure of 2,4,6,8,10-Undecapentaenoic acid, 5,9-dimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (2E,4E,6E,8E,10E)-, with its unique arrangement of double bonds and methyl groups, may confer particular properties or functions that are relevant to its biological activity or industrial applications.

6722-00-5

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6722-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6722-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,2 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6722-00:
(6*6)+(5*7)+(4*2)+(3*2)+(2*0)+(1*0)=85
85 % 10 = 5
So 6722-00-5 is a valid CAS Registry Number.

6722-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ro 11-0976

1.2 Other means of identification

Product number -
Other names 14'-Apo-β-carotinsaeure

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:6722-00-5 SDS

6722-00-5Relevant academic research and scientific papers

Synthesis of apocarotenoids by acyclic cross metathesis and characterization as substrates for human retinaldehyde dehydrogenases

Domínguez, Marta,Pequerul, Raquel,Alvarez, Rosana,Giménez-Dejoz, Joan,Birta, Eszter,Porté, Sergio,Rühl, Ralph,Parés, Xavier,Farrés, Jaume,de Lera, Angel R.

, p. 2567 - 2574 (2018/04/19)

A new synthesis of three apocarotenoids, namely 14′-apo-β-carotenal, 12′-apo-β-carotenal and 10′-apo-β-carotenal, has been achieved that is based on the acyclic cross-metathesis of the hexaene derived from retinal and the corresponding partners. These compounds can be enzymatically converted to their carboxylic acids by the human aldehyde dehydrogenases involved in retinaldehyde oxidation. Their kinetic parameters suggest that these enzymes might play a role in the physiological metabolism of apocarotenoids.

Synthesis and biological activities of higher homologues of retinoic acid

Winum,Kamal,Defacque,Commes,Chavis,Lucas,Marti,Montero

, p. 39 - 42 (2007/10/03)

Homoretinoic and bishomoretinoic acid have been synthesized. Fast reaction under ultrasonic activation (Wolff rearrangement, saponification) produced compounds in high yields. Only the bishomo analogue exhibits a significative activity alone and a synergi

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