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Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-α-L-rhamnopyranoside - CAS 940274-22-6

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Category
Main Product
Product Name
Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-α-L-rhamnopyranoside
Catalog Number
940274-22-6
Synonyms
Allyl 3-O-benzyl-2-O-p-tolylsulfonyl-a-L-rhamnopyranoside;Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-alpha-L-rhamnopyranoside
CAS Number
940274-22-6
Molecular Weight
448.53
Molecular Formula
C23H28O7S
COA
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MSDS
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Structure
CAS 940274-22-6 Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-α-L-rhamnopyranoside
Specification
Purity
95%
Reference Reading
1.Regioselective Alkoxycarbonylation of Allyl Phenyl Ethers Catalyzed by Pd/dppb Under Syngas Conditions.
Amézquita-Valencia M, Alper H. J Org Chem. 2016 Apr 14. [Epub ahead of print]
A simple and regioselective synthesis of phenoxy esters and phenylthio esters is reported. The products are obtained by selective alkoxycarbonylation catalyzed by Pd2(dba)3, 1,4-bis(diphenylphisphino)butane (dppb) and syngas (CO/H2) in chloroform/alcohol. This methodology affords bifunctional products in good yield with excellent n-selectivity, and without the need to use additives.
2.Tuning the adsorption behaviors of water, methanol, and ethanol in a porous material by varying the flexibility of substituted groups.
Sha Y1, Bai S2, Lou J1, Wu D1, Liu B1, Ling Y2. Dalton Trans. 2016 Apr 14. [Epub ahead of print]
Exploring the adsorption and separation of water, methanol, and ethanol is important concerning the use of a sustainable energy source from biofuel. In this paper, the effects of the flexibility of substituted groups have been studied based on three iso-reticular metal-organic frameworks (MOFs), in which the pore surface is decorated with propargyl (-CH2-C[triple bond, length as m-dash]CH), allyl (-CH2-CH[double bond, length as m-dash]CH2), and propyl (-CH2-CH2-CH3) groups respectively. These substituted groups stretch into the channel, acting as gates, and the gate-opening for guests is controlled by the flexibility as well as host-guest interactions. Our study results indicate that (i) the adsorption capacity of water, methanol and ethanol enhances accordingly with the increase of the flexibility of substituted groups; (ii) the adsorptive discrimination of water, methanol, and ethanol on this porous sorbent could be tuned by varying the substituted groups.
3.Allyl Isothiocyanate Induces Cell Toxicity by Multiple Pathways in Human Breast Cancer Cells.
Bo P1, Lien JC2, Chen YY3,4, Yu FS5, Lu HF6, Yu CS7, Chou YC8,9, Yu CC7, Chung JG1,10. Am J Chin Med. 2016 Apr;44(2):415-37. doi: 10.1142/S0192415X16500245.
Isothiocyanates (ITCs) occur in many cruciferous vegetables. These compounds, which have significant anticancer actions, can induce apoptosis in different human cancer cell lines. In the present study, we investigated if allyl isothiocyanate (AITC) would induce toxicity in human breast cancer MCF-7 (estrogen receptor positive) and MDA-MB-231 (estrogen receptor negative) cells. We found that AITC stimulated reactive oxygen species and Ca[Formula: see text] production, and decreased the mitochondrial membrane potential. Activity of caspase-8, -9 and -3 was increased by AITC in both cell lines. AITC also induced mitochondrial-mediated apoptosis, as shown by cytochrome c, AIF and Endo G release from mitochondria, activation of caspase-9 and caspase-3, and formation of DAPI-positive cells. There was a significant reduction in the levels of the anti-apoptotic protein Bcl-2 along with a marked increase in the pro-apoptotic protein Bax in both cell lines.
4.Different antibacterial activity of novel theophylline-based ionic liquids - Growth kinetic and cytotoxicity studies.
Borkowski A1, Ławniczak Ł2, Cłapa T3, Narożna D4, Selwet M3, Pęziak D2, Markiewicz B2, Chrzanowski Ł2. Ecotoxicol Environ Saf. 2016 Apr 12;130:54-64. doi: 10.1016/j.ecoenv.2016.04.004. [Epub ahead of print]
The aim of this study was to investigate novel theophylline-based ionic liquids and their cytotoxic effects towards model Gram-positive and Gram-negative bacteria (Bacillus cereus and Escherichia coli, respectively). Growth kinetics, respiratory rates and dehydrogenase activities were studied in the presence of ionic liquids at concentrations ranging from 10 to 1000mg/L. Additionally, the influence of ionic liquids on bacterial cells associated with specific interactions based on the structure of cell wall was evaluated. This effect was assessed by viability tests and scanning electron microscope observations. The obtained results confirmed that ionic liquids exhibit different levels of toxicity in relation to Gram-positive and Gram-negative bacteria. Those effects are associated with the chemical structure of the cationic species of the ionic liquids and their critical micelle concentration value. It was established that the presence of an alkyl or allyl group increased the toxicity, whereas the presence of an aryl group in the cation decreased the toxic effect of ILs.
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