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(4R)-2,2-dimethyl-4-[(E)-1-methyl-2-(3-phenoxyphenyl)ethenyl]-1,3-dioxolane is a chiral dioxolane derivative with a molecular formula of C20H24O3. It features a methyl and a phenyl group attached to the molecule and possesses a stereo center, resulting in two enantiomers, (R) and (S). This chemical compound is significant in the field of organic chemistry and is utilized in various applications across industry and research.

99566-51-5

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99566-51-5 Usage

Uses

Used in Pharmaceutical Synthesis:
(4R)-2,2-dimethyl-4-[(E)-1-methyl-2-(3-phenoxyphenyl)ethenyl]-1,3-dioxolane is used as a key intermediate in the synthesis of pharmaceuticals for its unique structural properties and chiral nature. Its ability to be incorporated into complex molecular frameworks makes it valuable in the development of new drugs with specific therapeutic effects.
Used in Agrochemical Development:
In the agrochemical industry, (4R)-2,2-dimethyl-4-[(E)-1-methyl-2-(3-phenoxyphenyl)ethenyl]-1,3-dioxolane serves as a crucial building block in the creation of novel compounds with pesticidal or herbicidal properties. Its chiral center allows for the development of enantioselective agrochemicals, which can target specific pests while minimizing harm to non-target organisms and the environment.
Used in Research and Development:
(4R)-2,2-dimethyl-4-[(E)-1-methyl-2-(3-phenoxyphenyl)ethenyl]-1,3-dioxolane is utilized in research settings to explore its chemical properties, reactivity, and potential applications in various chemical reactions. Its unique structure and chirality make it an interesting subject for studies in asymmetric synthesis, catalysis, and the development of new methodologies in organic chemistry.
Used in Organic Chemistry Education:
As a representative of chiral dioxolane derivatives, (4R)-2,2-dimethyl-4-[(E)-1-methyl-2-(3-phenoxyphenyl)ethenyl]-1,3-dioxolane is employed in educational settings to teach students about stereochemistry, asymmetric synthesis, and the importance of chirality in organic compounds. It serves as a practical example to illustrate concepts and techniques in organic chemistry courses.

Check Digit Verification of cas no

The CAS Registry Mumber 99566-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,6 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99566-51:
(7*9)+(6*9)+(5*5)+(4*6)+(3*6)+(2*5)+(1*1)=195
195 % 10 = 5
So 99566-51-5 is a valid CAS Registry Number.

99566-51-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R)-2,2-dimethyl-4-[(E)-1-(3-phenoxyphenyl)prop-1-en-2-yl]-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:99566-51-5 SDS

99566-51-5Relevant academic research and scientific papers

Absolute Structure and Activity Relationships of Cinnamyl Alcohol Derivatives of Pyrethroid Insecticides

Matsuo, Noritada,Yano, Toshihiko,Ohno, Nobuo

, p. 3029 - 3036 (2007/10/02)

Synthesis of three optically active pyrethroids containing cinnamyl-type alcohol moieties, and their insecticidal activity are reported.The presence of a m-phenoxy group at a benzene ring inverted the structure-activity relationships dramatically with respect to the absolute configuration of alcohol moieties.

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