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1,3-Dioxolane, 2-methyl-2-(3,4-pentadienyl)- (8CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20449-23-4

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20449-23-4 Usage

Chemical Structure

1,3-Dioxolane ring with a methyl group and a pentadienyl side chain

Explanation

The compound has a cyclic ether structure, specifically a 1,3-dioxolane ring, which consists of two oxygen atoms and two carbon atoms. Additionally, it has a methyl (CH3) group and a pentadienyl side chain (a chain with three carbon-carbon double bonds).

Explanation

Due to its polar nature, 1,3-Dioxolane, 2-methyl-2-(3,4-pentadienyl)(8CI) can dissolve a variety of substances, making it a useful solvent in chemical reactions.

Explanation

The compound's unique structure and properties make it suitable for use in various industries, including the synthesis of pharmaceuticals, the creation of perfumes, and the development of flavorings for the food and beverage industry.

Explanation

The compound can act as a building block or reactant in the formation of other organic compounds, contributing to its importance in the field of organic chemistry.

Explanation

1,3-Dioxolane, 2-methyl-2-(3,4-pentadienyl)(8CI) has a pleasant, sweet smell, which can be useful in the perfume industry.

Explanation

The compound is highly flammable, which means it can easily catch fire when exposed to a source of ignition. This property requires careful handling and storage to prevent accidents.

Explanation

Due to its flammable nature and potential toxic effects, it is crucial to handle and store 1,3-Dioxolane, 2-methyl-2-(3,4-pentadienyl)(8CI) with caution, following safety guidelines to minimize the risk of exposure and accidents.

Solvent

Commonly used as a solvent

Applications

Used in the production of pharmaceuticals, perfumes, and flavorings

Synthesis

Used in the synthesis of other organic compounds

Odor

Sweet odor

Flammability

Flammable in nature

Health Hazards

May pose health hazards if not properly handled and stored

Check Digit Verification of cas no

The CAS Registry Mumber 20449-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,4 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20449-23:
(7*2)+(6*0)+(5*4)+(4*4)+(3*9)+(2*2)+(1*3)=84
84 % 10 = 4
So 20449-23-4 is a valid CAS Registry Number.

20449-23-4Downstream Products

20449-23-4Relevant academic research and scientific papers

Cobalt-Catalyzed Regio- and Stereoselective Hydroboration of Allenes

Guo, Yinlong,Huang, Zheng,Li, Can,Ma, Shengming,Wang, Lei,Yang, Zheng

, p. 6278 - 6283 (2020)

An efficient pincer-ligand-based cobalt-complex-catalyzed allene hydroboration affording Z-allylic boronates is described. The reaction demonstrates an excellent regio- as well as Z-stereoselectivity and a wide substrate scope that tolerates many functional groups. Based on solvent-assisted electrospray ionization mass spectrometry (SAESI-MS) studies, a rationale for the cobalt-catalyzed hydroboration involving the highly selective insertion of an allene into the Co?H bond to form Z-allylic cobalt intermediates is proposed.

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