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2,2-Dimethyl-4H-1,3-dioxin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87769-48-0

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87769-48-0 Usage

Synthesis Reference(s)

Synthesis, p. 224, 1985 DOI: 10.1055/s-1985-31167

Check Digit Verification of cas no

The CAS Registry Mumber 87769-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,6 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87769-48:
(7*8)+(6*7)+(5*7)+(4*6)+(3*9)+(2*4)+(1*8)=200
200 % 10 = 0
So 87769-48-0 is a valid CAS Registry Number.

87769-48-0Relevant articles and documents

INSECTICIDAL CYCLIC CARBONYL AMIDINES

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Page/Page column 35, (2010/04/03)

Disclosed are compounds of Formula (I), including all stereoisomers, and salts thereof, wherein Y is O, S, NR5 or CR3R4, G is a direct bond, and Z is CR3R4 or NR5; or Y is CR3R4, G is a direct bond, and Z is O or S; or Y is O, S, NR5 or CR3R4, G is CR3R4, and Z is O, S, NR5 or CR3R4; or Y is O, and G–Z is CH=CH; or Y–G is CH=CH, and Z is O, S or NR5; and R1, R2, R3, R4, R5 and Q are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.

Process for producing 1,3-dioxin-4-one derivatives

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, (2008/06/13)

A process for producing 1,3-dioxin-4-one derivatives having a lower alkyl group at 2-position and useful as a starting raw material for prostaglandins, with a high yield is provided, which process comprises reacting formyl Meldrum's acid with a lower aliphatic carbonyl compound of 2 to 4 carbon atoms in a solvent containing the carbonyl compound at 100° to 120° C., while portionwise adding the acid into the solvent, the total quantity of the acid added being 0.2 mol or less per liter of the solvent.

SYNTHESIS OF 1,3-DIOXIN-4-ONES UNSUBSTITUTED AT THE 5- AND 6-POSITIONS AND THEIR PHOTOADDITION TO ALKENES

Sato, Masayuki,Ogasawara, Hiromichi,Sekiguchi, Keiko,Kaneko, Chikara

, p. 2563 - 2570 (2007/10/02)

A general synthetic method of 5,6-unsubstituted 1,3-dioxin-4-ones and their photoaddition to alkenes are described.The photoadducts thus obtained were found to give, merely by refluxing in water, alkanes having carboxaldehyde and acetic acid appendages at the vicinal position.

Synthesis of 1,3-dioxin-4-one Derivatives

Sato, Masayuki,Ogasawara, Hiromichi,Oi, Keiichi,Kato, Tetsuzo

, p. 1896 - 1901 (2007/10/02)

A facile and general synthesis of 2,2-dimethyl-1,3-dioxin-4-one derivatives (1) is reported.Treatment of β-keto acids with a mixture of isopropenyl acetate and conc. sulfuric acid gave 2,2-dimethyl-1,3-dioxin-4-ones (1).Similar treatment of tert-butyl esters of β-keto acids also gave 1.KEYWORDS - 2,2-dimethyl-1,3-dioxin-4-one derivative; diketene-acetone adduct; diketene; acylketene; β-keto acid; β-keto ester

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