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Heneicos-1-ene is an organic compound with the molecular formula C21H40, consisting of a 21-carbon alkene chain with a double bond at the first carbon atom. It is a linear, unbranched hydrocarbon belonging to the alkene class, which is characterized by the presence of a carbon-carbon double bond. Heneicos-1-ene is a colorless liquid with a relatively high boiling point due to its long carbon chain. It is an isomer of heneicosane, a 21-carbon alkane, and can be used as a precursor in the synthesis of various organic compounds. The compound is not widely used in commercial applications but serves as an example of the vast diversity of hydrocarbon structures and their properties.

1599-68-4

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1599-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1599-68-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1599-68:
(6*1)+(5*5)+(4*9)+(3*9)+(2*6)+(1*8)=114
114 % 10 = 4
So 1599-68-4 is a valid CAS Registry Number.

1599-68-4Downstream Products

1599-68-4Relevant 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 (1985)

- 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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