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(Z)-2-Hydroxy-nonadec-10-enenitrile is a chemical compound with the molecular formula C19H33NO. It is an organic molecule characterized by a hydroxyl group (-OH) at the 2nd carbon position, a nitrile group (-CN) at the 10th carbon position, and a double bond (C=C) between the 10th and 11th carbon atoms in the Z configuration. (Z)-2-Hydroxy-nonadec-10-enenitrile is a member of the alkenes class, which are hydrocarbons containing at least one carbon-carbon double bond. The presence of the hydroxyl and nitrile groups imparts unique chemical properties to this molecule, making it potentially useful in various applications such as the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals.

81861-40-7

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81861-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81861-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,6 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81861-40:
(7*8)+(6*1)+(5*8)+(4*6)+(3*1)+(2*4)+(1*0)=137
137 % 10 = 7
So 81861-40-7 is a valid CAS Registry Number.

81861-40-7Downstream Products

81861-40-7Relevant academic research and scientific papers

Darmstoff Analogues. 2. Ring and Side-Chain Effects on Smooth-Muscle Contraction

Wiley, Robert A.,Harris, Wayne T.,Brungardt, Catherine,Marx, Michael

, p. 121 - 125 (2007/10/02)

2-cis-Δ8-Heptadecenyl-4-(hydroxymethyl)-1,3-dioxolane monosodium phosphate (1b) has been shown to be present as a major component of Darmstoff in mammalian intestine and to be a potent inducer for contraction of intestinal smooth muscle.The analogous 2-pentadecyl material 1a, also found abundantly in the intestine, is inactive.In this study, synthesis of phosphorylated hydroxymethyl-1,4-dioxanes, -tetrahydrofurans, -cyclopentanes, and -oxathiolanes bearing both oleyl and palmityl side chains is reported.Of these, 2-(hydroxymethyl)-5-cis-Δ8-heptadecenyl-1,4-dioxane monosodium phosphate (2b) exhibits about 12percent of the activity of 1b.Its pentadecyl analogue 2a, like 1a, is totally inactive, as are all other compounds prepared.The results indicate that Darmstoff-like compounds exhibit specific chemical requirements for activity and that where activity is encountered, the side-chain specificity noted in 1a and 1b can be preserved.

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