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1,4-dimethoxy-2-(3-methylbut-2-en-1-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79233-13-9

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79233-13-9 Usage

Structure

Benzene derivative with two methoxy groups and a 3-methylbut-2-en-1-yl side chain

Usage

Primarily used as a research chemical

Common Applications

Not commonly found in consumer products

Similar Compounds

Used as fragrances or flavoring agents

Industry Documentation

Exact uses and applications are not well-documented

Precautions

Should be taken when handling in the laboratory due to intricate structure and potential reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 79233-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,3 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79233-13:
(7*7)+(6*9)+(5*2)+(4*3)+(3*3)+(2*1)+(1*3)=139
139 % 10 = 9
So 79233-13-9 is a valid CAS Registry Number.

79233-13-9Relevant academic research and scientific papers

Electrophilic allylation of arenes with in situ generated allyltriarylbismuthonium compound: The Bismuth-mediated polarity inversion of allylsilanes

Matano, Yoshihiro,Yoshimune, Masanori,Suzuki, Hitomi

, p. 7475 - 7478 (2007/10/02)

Reaction of triarylbismuth difluorides 1 with allyltrimethylsilane 2 in CH2Cl2 in the presence of BF3·OEt2 at low temperature generates allyltriarylbismuthonium compound 3 as a pale yellow solution, in which aromatic hydrocarbons and ethers, triphenylphosphine, dimethyl sulfide, p-toluenesulfinate, and thiophenol are all readily allylated to afford the corresponding allyl derivatives in moderate to good yields.

Total synthesis of 2-tetraprenylbenzoquinol and -benzoquinone

Bouzbouz,Kirschleger

, p. 714 - 718 (2007/10/02)

The total synthesis of 2-tetraprenylbenzoquinol and -benzoquinone is described. A key step in this synthesis is the highly regio- and stereoselective coupling between an appropriate aromatic allylcarbonate and an activated bifunctional farnesyl derivative

AN EFFICIENT REGIO- AND STEREOSPECIFIC ALKENYLATION OF PHENOLIC ETHERS BY PRENYL AND GERANYL DIISOPROPYL PHOSPHATES

Araki, Shuki,Manabe, Shin-ichi,Butsugan, Yasuo

, p. 797 - 800 (2007/10/02)

Prenyl and geranyl diisopropyl phosphates readily alkenylate a variety of phenolic ethers regio- and stereospecifically without any appreciable side reactions.

Acid-catalysed Intramolecular Cyclization of Geranyl Hydroquinone Derivatives from Cordia alliodora. X-Ray Crystal and Molecular Structure of 1,2,3,3a,4,9,10,10a-Octahydro-5,8-dimethoxy-3,10-dimethyl-3a,9-epoxybenzazulene

Manners, Gary D.,Wong, Rosalind Y.

, p. 1849 - 1854 (2007/10/02)

The aqueous acid-catalysed intramolecular cyclization of dimethylated alliodorin (2) obtained from the heartwood of Cordia alliodora has been characterized by X-ray analysis as the unusual tetracyclic di-O-methyl hydroquinone title compound (8).A new synthesis of di-O-methylalliodorin (2) from a terminal methylallylic sulphide derivative of 2-geranil-1,4-dimethoxybenzene is described. Crystals of the title compound (8) are monoclinic, space group P21/c, unit cell dimensions a = 14.984(7), b = 5.206(4), c = 20.131(9) Angstroem, β = 99.77(1) deg, Z = 4.The structure was solved by direct methods and refined by least-squares calculations to an R value of 0.078 for 1 832 independent reflections measured on a diffractometer using Cu-Kα radiation.

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