Welcome to LookChem.com Sign In|Join Free

CAS

  • or

50906-59-7

Post Buying Request

50906-59-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

50906-59-7 Usage

Description

(2E,6E)-8-(2,5-Dihydroxyphenyl)-2,6-dimethyl-2,6-octadienal is an organic compound with the molecular formula C16H20O3. It is a polyunsaturated aldehyde characterized by a long hydrocarbon chain and two conjugated double bonds. The presence of a hydroxyl group on the phenyl ring contributes to its chemical reactivity. This versatile compound can be synthesized or extracted from natural sources and may have potential industrial or biological applications.

Uses

Used in Flavoring Industry:
(2E,6E)-8-(2,5-Dihydroxyphenyl)-2,6-dimethyl-2,6-octadienal is used as a flavoring agent due to its unique chemical structure and reactivity, which can impart specific taste and aroma profiles to various products.
Used in Synthesis of Organic Compounds:
In the chemical industry, (2E,6E)-8-(2,5-Dihydroxyphenyl)-2,6-dimethyl-2,6-octadienal serves as a precursor in the synthesis of other organic compounds, leveraging its reactive functional groups and structural features.
Used in Antioxidant Applications:
Due to its structural features, (2E,6E)-8-(2,5-Dihydroxyphenyl)-2,6-dimethyl-2,6-octadienal may exhibit antioxidant properties, making it a potential candidate for use in applications requiring the prevention of oxidative damage or the enhancement of shelf life in various products.
Used in Bioactive Compound Research:
(2E,6E)-8-(2,5-Dihydroxyphenyl)-2,6-dimethyl-2,6-octadienal's potential bioactivity, possibly due to its phenolic hydroxyl group and conjugated double bonds, positions it for research and development in the field of bioactive compounds, which could lead to applications in pharmaceuticals or health supplements.

Check Digit Verification of cas no

The CAS Registry Mumber 50906-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,0 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50906-59:
(7*5)+(6*0)+(5*9)+(4*0)+(3*6)+(2*5)+(1*9)=117
117 % 10 = 7
So 50906-59-7 is a valid CAS Registry Number.

50906-59-7SDS

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 alliodorine EE

1.2 Other means of identification

Product number -
Other names Alliodorin

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:50906-59-7 SDS

50906-59-7Relevant articles and documents

Microwave-assisted efficient synthesis of alliodorin and (±)- curcuhydroquinone

Kad, Goverdhan L.,Khurana, Anupam,Singh, Vasundhara,Singh, Jasvinder

, p. 164 - 165 (2007/10/03)

Terpenoids 1 and 2 have been synthesized from readily available starting materials using Li2CuCl4-catalysed coupling of Grignard reagents with alkyl/aryl bromides and microwave-assisted oxidation of allylic methyl groups, using SeOs

PREMIERE SYNTHESE TOTALE DE L'ALLIODORINE. PREPARATION D'ALDEHYDES ISOPRENIQUES E A PARTIR DES METHYL-2 OXO-6 HEXENE-2 (E + Z) CARBONITRILES-1.

Tortajada, J.,Morizur, J-P.

, p. 253 - 262 (2007/10/02)

The first synthesis of alloiodorine 4EE, a constituent isolated from the duramen of a tropical tree: Cordia alliodora is reported.A mixture of E and Z isomers of 2-methyl-6-oxo-2-heptenenitrile 3 easily accesible by U.V. irradiation of 1-methyl-2-oxo-cyclopentanecarbonitrile 2 is used as starting material.E/Z isomerism is suppressed during a step of the synthesis reduction of the α,β-unsaturated nitrile function (E + Z) in the α,β-unsaturated aldehyde E ( the Z -> E isomerisation occurs during the hydrolysis of the internediate imine).The synthesis was conducted in six steps with an overall yield of 12,5percent from 1-methyl-2-oxo-cyclopentanecarbonitrile 2.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 50906-59-7