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1-(trimethylsilyl)-1,7-octadiyne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83182-85-8

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83182-85-8 Usage

Structure

A derivative of octyne with a trimethylsilyl group attached to one end of the molecule

Alkynes

Two carbon-carbon triple bonds

Silyl group

A trimethylsilyl group (SiMe3)

Organic synthesis

Building block for various compounds

Pharmaceutical industry

Used in the preparation of pharmaceuticals

Agrochemicals

Employed in the synthesis of agrochemicals

Materials

Utilized in the development of new materials

Versatile compound

Capable of undergoing various chemical reactions

Valuable tool

Important in organic chemistry for its unique properties and reactivity

Synthetic methodologies

Contributes to the development of new synthetic methodologies

Complex organic molecules

Facilitates the production of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 83182-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83182-85:
(7*8)+(6*3)+(5*1)+(4*8)+(3*2)+(2*8)+(1*5)=138
138 % 10 = 8
So 83182-85-8 is a valid CAS Registry Number.

83182-85-8Relevant academic research and scientific papers

Total synthesis of an exceptional brominated 4-pyrone derivative of algal origin: An exercise in gold catalysis and alkyne

Hoffmeister, Laura,Fukuda, Tsutomu,Pototschnig, Gerit,Frstner, Alois

, p. 4529 - 4533 (2015)

A concise approach to the algal metabolite 1 is described, which also determines the previously unknown stereostructure of this natural product. Compound 1 is distinguished by a rare brominated 4-pyrone nucleus linked as a ketene-acetal to a polyunsaturated macrocyclic scaffold comprising an extra homoallylic bromide entity. The synthesis of 1 is based on the elaboration and selective functionalization of the linear precursor 23 endowed with no less than six different sites of unsaturation including the highly enolized oxo-alkanoate function. Key to success was the formation of the 2-alkoxy-4-pyrone ring by a novel gold-catalyzed transformation which engages only the acetylenic β-ketoester substructure of 23 but leaves all otherπ-bonds untouched. The synthesis was completed by a ring-closing alkyne metathesis to forge the signature cycloalkyne motif of 1 followed by selective bromination of the ketene-acetal site in the resulting product 27 without touching the skipped diene-yne substructure resident within the macrocyclic tether.

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