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2-Methyl-2-tridecyl-[1,3]dioxolane is a cyclic organic compound characterized by a 1,3-dioxolane ring, which consists of two oxygen atoms and three carbon atoms. The compound features a methyl group attached to the second carbon of the ring and a tridecyl (C13H27) alkyl chain attached to the same carbon. This structure imparts unique properties to the molecule, making it potentially useful in various chemical applications, such as solvents, fragrances, or intermediates in the synthesis of other organic compounds. Its specific chemical formula is C17H34O2, and it is a colorless liquid with a molecular weight of 270.45 g/mol.

4353-03-1

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4353-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4353-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4353-03:
(6*4)+(5*3)+(4*5)+(3*3)+(2*0)+(1*3)=71
71 % 10 = 1
So 4353-03-1 is a valid CAS Registry Number.

4353-03-1Downstream Products

4353-03-1Relevant academic research and scientific papers

SELECTIVE MIXED COUPLING OF CARBOXYLIC ACIDS (II). -PHOTOLYSIS OF UNSYMMETRICAL DIACYLPEROXIDES WITH ALKENYL-, HALO-, KETO-, CARBOXYL-GROUPS AND A CHIRAL α-CARBON. COMPARISON WITH THE MIXED KOLBE ELECTROLYSIS.

Feldhues, Michael,Schaefer, Hans J.

, p. 4213 - 4236 (2007/10/02)

- Alkenoyl and functionalized alkanoyl dodecanoyl peroxides are prepared in 70 to 97 percent yield and photolyzed at -78 deg C.Thereby 4- to 10-alkenoyl and 4-alkynoyl peroxides afford good yields (56 - 68 percent) of unsymmetrical coupling products.Similarly α- to δ-haloalkanoyl, cholanoyl or 3- and 4-carboxyalkanoyl peroxides can be coupled (40 - 70 percent).The α-chiral diacyl peroxide 1s undergoes the photochemical coupling reaction with 80 percent retention of its configuration.The photolysis of diacyl peroxides at -78 deg C proves to be a favorable supplement of the Kolbe-electrolysis in cases, where the electrolysis fails or produces low yields.

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