17966-13-1 Usage
Description
(Z)-11-[(2R,3S)-3-pentyloxiran-2-yl]undec-9-enoic acid is a complex organic compound with a unique molecular structure, characterized by the presence of a Z-configuration double bond at the 9th carbon and a 3-pentyloxiran-2-yl group attached to the 11th carbon. This molecule exhibits a high degree of structural specificity, which may contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(Z)-11-[(2R,3S)-3-pentyloxiran-2-yl]undec-9-enoic acid is used as a pharmaceutical compound for its potential therapeutic properties. The specific molecular structure of this compound may allow it to interact with biological targets, such as receptors or enzymes, in a unique manner, leading to potential applications in the treatment of various diseases.
Used in Cosmetic Industry:
In the cosmetic industry, (Z)-11-[(2R,3S)-3-pentyloxiran-2-yl]undec-9-enoic acid may be used as an active ingredient in skincare products due to its potential to modulate skin cell functions and improve skin health. The compound's unique structure could provide benefits such as anti-aging, moisturizing, or anti-inflammatory effects.
Used in Chemical Synthesis:
(Z)-11-[(2R,3S)-3-pentyloxiran-2-yl]undec-9-enoic acid can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structural features may be exploited to create novel molecules with specific properties, which could be applied in various industries, such as pharmaceuticals, agrochemicals, or materials science.
Used in Biofeedstock Research:
As a potentially useful biofeedstock, (Z)-11-[(2R,3S)-3-pentyloxiran-2-yl]undec-9-enoic acid may be studied for its potential to be converted into valuable chemicals or materials through biological or chemical processes. This could contribute to the development of sustainable and environmentally friendly production methods for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 17966-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,6 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17966-13:
(7*1)+(6*7)+(5*9)+(4*6)+(3*6)+(2*1)+(1*3)=141
141 % 10 = 1
So 17966-13-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H32O3/c1-2-3-10-13-16-17(21-16)14-11-8-6-4-5-7-9-12-15-18(19)20/h8,11,16-17H,2-7,9-10,12-15H2,1H3,(H,19,20)/b11-8-/t16-,17+/m0/s1
17966-13-1Relevant articles and documents
Molecular characterization of NbEH1 and NbEH2, two epoxide hydrolases from Nicotiana benthamiana
Huang, Fong-Chin,Schwab, Wilfried
, p. 6 - 15 (2013/07/11)
Plant epoxide hydrolases (EH) form two major clades, named EH1 and EH2. To gain a better understanding of the biochemical roles of the two classes, NbEH1.1 and NbEH2.1 were isolated from Nicotiana benthamiana and StEH from potato and heterologously expressed in Escherichia coli. The purified recombinant proteins were assayed with a variety of substrates. NbEH1.1 only accepted some aromatic epoxides, and displayed the highest enzyme activity towards phenyl glycidyl ether. In contrast, NbEH2.1 displayed a broad substrate range and similar substrate specificity as StEH. The latter enzymes showed activity towards all fatty acid epoxides examined. The activity (Vmax) of NbEH1.1 towards phenyl glycidyl ether was 10 times higher than that of NbEH2.1. On the contrary, NbEH2.1 converted cis-9,10-epoxystearic acid with Vmax of 3.83 μmol min mg-1 but NbEH1.1 could not hydrolyze cis-9,10- epoxystearic acid. Expression analysis revealed that NbEH1.1 is induced by infection with tobacco mosaic virus (TMV) and wounding, whereas NbEH2.1 is present at a relatively constant level, not influenced by treatment with TMV and wounding. NbEH1.1 transcripts were present predominantly in roots, whereas NbEH2.1 mRNAs were detected primarily in leaves and stems. Overall, these two types of tobacco EH enzymes are distinguished not only by their gene expression, but also by different substrate specificities. EH1 seems not to participate in cutin biosynthesis and it may play a role in generating signals for activation of certain defence and stress responses in tobacco. However, members of the EH2 group hydrate fatty acid epoxides and may be involved in cutin monomer production in plants.
