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56904-85-9

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56904-85-9 Usage

General Description

2,4-OCTADIEN-1-OL, a chemical compound with the molecular formula C8H14O, is an unsaturated alcohol that is commonly used in fragrance and flavoring applications. It is a colorless liquid with a fruity, floral odor, and is often used as a scent in perfumes and personal care products. Additionally, 2,4-OCTADIEN-1-OL is used in the food industry as a flavoring agent, providing a sweet and fruity taste to various products. Its versatile nature also allows it to be used as a starting material in the synthesis of other organic compounds, making it an important chemical in the production of various consumer goods.

Check Digit Verification of cas no

The CAS Registry Mumber 56904-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,0 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56904-85:
(7*5)+(6*6)+(5*9)+(4*0)+(3*4)+(2*8)+(1*5)=149
149 % 10 = 9
So 56904-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O/c1-2-3-4-5-6-7-8-9/h4-7,9H,2-3,8H2,1H3

56904-85-9 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A16820)  2,4-Octadien-1-ol, 95%   

  • 56904-85-9

  • 1g

  • 494.0CNY

  • Detail
  • Alfa Aesar

  • (A16820)  2,4-Octadien-1-ol, 95%   

  • 56904-85-9

  • 5g

  • 1985.0CNY

  • Detail

56904-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-OCTADIEN-1-OL

1.2 Other means of identification

Product number -
Other names FEMA 3956

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:56904-85-9 SDS

56904-85-9Relevant articles and documents

Cobalt-Catalyzed Diastereo- And Enantioselective Reductive Allyl Additions to Aldehydes with Allylic Alcohol Derivatives via Allyl Radical Intermediates

Wang, Lei,Wang, Lifan,Li, Mingxia,Chong, Qinglei,Meng, Fanke

, p. 12755 - 12765 (2021/08/30)

Catalytic generation of ambiphilic π-allyl-metal complexes and their utility in enantioselective transformations constitutes a powerful approach for introduction of allyl groups to a molecule. Herein an unprecedented cobalt-catalyzed highly site-, diastereo-, and enantioselective protocol for stereoselective formation of nucleophilic allyl-Co(II) complexes followed by addition to aldehydes is presented. The reaction features diastereo- and enantioconvergent conversion of easily accessible allylic alcohol derivatives to diversified enantioenriched homoallylic alcohols with a remarkably broad scope of allyl groups that can be introduced. Mechanistic studies indicated that allyl radical intermediates were involved in this process. These new discoveries establish a new strategy for development of enantioselective transformations through capture of radicals by chiral Co complexes, pushing forward the frontier of Co complexes for enantioselective catalysis.

Cobalt-catalyzed versus uncatalyzed intramolecular Diels-Alder cycloadditions

Biletskyi, Bohdan,Tenaglia, Alphonse,Clavier, Hervé

supporting information, p. 103 - 107 (2017/12/28)

The intramolecular [4+2] cycloadditions of dienynes was investigated using cobalt-based catalysts. Substrates without substitution on alkyne moiety were found to react under thermal activation. The use of a cobalt salt as catalyst made reactions cleaner by limiting the formation of byproducts. Cycloadditions with dienynes possessing a substituent on the alkyne pattern occurred only in presence of a cobalt catalyst which displayed a moderate to good activity depending on the substrate patterns.

Aggregation behavior of tetraenoic fatty acids in aqueous solution

Wang, Yonghui,Ma, Jianguo,Cheon, Hwan-Sung,Kishi, Yoshito

, p. 1333 - 1336 (2008/04/05)

(Chemical Equation Presented) Why so blue? Unique blue-shifted UV absorptions were used to follow the aggregation of C24 tetraene fatty acids in aqueous solution. Aggregation takes place through three distinct states (i.e. K→T1→T2; see picture). It is suggested that all of these aggregates are lamellar-type in a local sense but differ in the packing mode of the fatty acid backbone.

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