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16,16-Diethoxy-3,5-hexadecadiyne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71673-31-9

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71673-31-9 Usage

Type of compound

Diynyl compound

Functional groups

Ethoxy (C2H5O), indicating it is an ether compound

Physical state

Colorless liquid

Usage

Research and development in various industries

Potential applications

Materials science and pharmaceuticals

Unique structure

Contains two carbon-carbon triple bonds

Synthesis

Can be used as a building block for more complex organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 71673-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,7 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71673-31:
(7*7)+(6*1)+(5*6)+(4*7)+(3*3)+(2*3)+(1*1)=129
129 % 10 = 9
So 71673-31-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O2/c1-4-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21-5-2)22-6-3/h20H,4-6,11-19H2,1-3H3

71673-31-9Downstream Products

71673-31-9Relevant academic research and scientific papers

Method for Producing Asymmetric Conjugated Diyne Compound and Method for Producing Z,Z-Conjugated Diene Compound Using the Same

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Paragraph 0072; 0073, (2016/09/12)

Provided are a method for efficiently producing an asymmetric conjugated diyne from an inexpensive and safe alternative compound to hydroxylamine hydrochloride and a method for producing a Z,Z-conjugated diene compound from the asymmetric conjugated diyne compound thus obtained. More specifically, provided is a method for producing an asymmetric conjugated diyne compound comprising a step of subjecting a terminal alkyne compound (1): HC≡C—Z1—Y1 to a coupling reaction with an alkynyl halide (2) Y2—Z2—C≡C—X by using sodium borohydride in water and an organic solvent in the presence of a copper catalyst and a base to obtain the asymmetric conjugated diyne compound (3): Y2—Z2—C≡C—C≡C—Z1—Y1. In addition, provided is a method for producing a Z,Z-conjugated diene compound by reducing the resulting asymmetric conjugated diyne compound, or the like.

SYNTHETIC NAVEL ORANGEWORM PHEROMONE COMPOSITION AND METHODS RELATING TO PRODUCTION OF SAME

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Page/Page column 12; 13, (2010/05/13)

One or more embodiments of the invention are directed to the synthetic methods for making lepidopteran pheromones including navel orangeworm pheromones. The synthetic methods involve novel, efficient, and environmentally benign steps and procedures.

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