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Undecanoic acid, 11-[3-(3H-diazirin-3-yl)phenoxy]-, methyl ester is a complex organic compound with the chemical formula C20H27N2O3. It is a derivative of undec-11-enoic acid, featuring a phenoxy group substituted with a 3H-diazirin-3-yl moiety at the 3-position. The diazirine ring is a strained three-membered ring containing two nitrogen atoms, which makes it highly reactive and useful in photoaffinity labeling. Undecanoic acid, 11-[3-(3H-diazirin-3-yl)phenoxy]-, methyl ester is typically used in biochemical research as a photoreactive probe to study protein-lipid interactions. The methyl ester group allows for easier incorporation into biological systems, and upon UV irradiation, the diazirine group can form covalent bonds with nearby amino acid residues, facilitating the identification and characterization of protein targets.

65114-62-7

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65114-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65114-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,1 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65114-62:
(7*6)+(6*5)+(5*1)+(4*1)+(3*4)+(2*6)+(1*2)=107
107 % 10 = 7
So 65114-62-7 is a valid CAS Registry Number.

65114-62-7Downstream Products

65114-62-7Relevant 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 (1982)

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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