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Undecanoic acid, 11-[3-(3H-diazirin-3-yl)phenoxy]-, also known as 11-[3-(3H-diazirin-3-yl)phenoxy]undecanoic acid, is a chemical compound with the molecular formula C17H23N3O3. It is a derivative of undec-11-enoic acid, featuring a phenoxy group at the 11th position, which is substituted with a 3H-diazirin-3-yl group. Undecanoic acid, 11-[3-(3H-diazirin-3-yl)phenoxy]- is of interest in chemical research due to its unique structure and potential applications in various fields, such as pharmaceuticals and materials science. The diazirine group, in particular, is known for its photoreactive properties, making it a valuable tool in photoaffinity labeling and other photochemical reactions.

80863-12-3

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80863-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80863-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,6 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80863-12:
(7*8)+(6*0)+(5*8)+(4*6)+(3*3)+(2*1)+(1*2)=133
133 % 10 = 3
So 80863-12-3 is a valid CAS Registry Number.

80863-12-3Downstream Products

80863-12-3Relevant academic research and scientific papers

Sites of Photolytic Intermolecular Cross-Linking between Fatty Acyl Chains in Phospholipids Carrying a Photoactivable Carbene Precursor

Radhakrishnan, Ramachandran,Costello, Catherine E.,Khorana, H. Gobind

, p. 3990 - 3997 (2007/10/02)

A number of sn-glycero-3-phosphorylcholines containing the photosensitive ω-undecanoyl group in the sn-2 position and a dideuterated palmitic or stearic acid with both deuteriums on specific carbon atoms along the hydrocarbon chain in the sn-1 position were synthesized.Photolysis of either sonicated vesicles or multilamellar dispersions prepared from these synthetic phospholipids gave extensive intermolecularly cross-linked products.The distribution of the sites of cross-linking was determined by an analysis of cross-linked dimeric fatty esters by using low-resolution electron impact mass spectrometry.The predominance of the benzylic cleavage with a γ-hydrogen abstraction in the mass spectra of these diesters rendered such a quantitation relatively easy.Mass spectral analysis showed that there is a broad distribution in the cross-linking positions along the deuterated sn-1 chain, with the amount of cross-linking increasing toward the hydrophobic core of the bilayer.These results are in agreement with the conformational mobility of the fatty acyl chains and the localization of the photosensitive diazirinophenoxy group in the middle of the bilayer.

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