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13071-59-5

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13071-59-5 Usage

General Description

1-O-Benzyl-rac-glycerol, also known as Benzyl glycerol, is a synthetic chemical compound used in scientific research, particularly in the field of organic chemistry. It is an organic compound with a benzene ring attached to a glycerol molecule through an oxygen atom. It's often used as a chemical reagent or intermediate. Its molecular formula is C10H12O3 and it's known for its stability under standard temperature and pressure. Although it has a wide range of potential applications, extensive safety data is not currently available. Specific care should be taken to handle it properly in line with good laboratory practice.

Check Digit Verification of cas no

The CAS Registry Mumber 13071-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,7 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13071-59:
(7*1)+(6*3)+(5*0)+(4*7)+(3*1)+(2*5)+(1*9)=75
75 % 10 = 5
So 13071-59-5 is a valid CAS Registry Number.

13071-59-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-BENZYL-RAC-GLYCEROL

1.2 Other means of identification

Product number -
Other names 1-BENZYLGLYCEROL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13071-59-5 SDS

13071-59-5Relevant articles and documents

ALTERNATIVE, SIMPLE ROUTE TO HYDROXYMETHYL CROWN ETHERS

Ctech, Bronislav

, p. 4197 - 4198 (1980)

Components for polymer-supported catalysts, hydroxymethyl-substituted 15-crown-5 and 18-crown-6 were prepared from readily available starting materials on relative simple way.

Synthesis and vesicle formation from dimeric pseudoglyceryl lipids with (CH2)m spacers: Pronounced m-value dependence of thermal properties, vesicle fusion, and cholesterol complexation

Bhattacharya, Santanu,De, Soma

, p. 2335 - 2347 (1999)

Eight new dimeric lipids, in which the two Me2N+ ion headgroups are separated by a variable number of polymethylene units [-(CH2)m-], have been synthesized. The electron micrograph (TEM) and dynamic light scattering (DLS) of their aqueous dispersions confirmed the formation of vesicular-type aggregates. The vesicle sizes and morphologies were found to depend strongly on the m value, the method, and thermal history of the vesicle preparation. Information on the thermotropic properties of the resulting vesicles was obtained from microcalorimetry and temperature-dependent fluorescence anisotropy measurements. Interestingly, the Tm values for these vesicles revealed a nonlinear dependence on spacer chain length (m value). These vesicles were able to entrap riboflavin. The rates of permeation of the OH- ion under an imposed transmembrane pH gradient were also found to depend significantly on the m value. X-Ray diffraction of the cast films of the lipid dispersions elucidated the nature and the thickness of these membrane organizations, and it was revealed that these lipids organize in three different ways depending on the m value. The EPR spin-probe method with the doxylstearic acids 5NS, 12NS, and 16NS, spin-labeled at various positions of stearic acid, was used to establish the chain-flexibility gradient and homogeneity of these bilayer assemblies. The apparent fusogenic propensities of these bipolar tetraether lipids were investigated in the presence of Na2SO4 with fluorescence-resonance energy-transfer fusion assay. Small unilamellar vesicles formed from 1 and three representative biscationic lipids were also studied with fluorescence anisotropy and 1H NMR spectroscopic techniques in the absence and the presence of varying amounts of cholesterol.

Percarboxylic Acid Oxidation of α-Hydroxy-Substituted Alkoxyallenes: The Unexpected Formation of Acyloxy-Substituted 1,2-Diketones and the Synthesis of Functionalized Quinoxalines

Klemme, Robby,Bentz, Christoph,Zukowski, Tomasz,Schefzig, Luise,Lentz, Dieter,Reissig, Hans-Ulrich,Zimmer, Reinhold

, p. 1491 - 1501 (2016)

Treatment of α-hydroxy-substituted methoxyallene derivatives with meta-chloroperbenzoic acid provided acyloxy-substituted 1,2-diketones in moderate yields. A mechanism for the formation of these unexpected products is proposed. The configuration of the enantiopure compound (S)-1-(3-methylquinoxalin-2-yl)-1-(4-nitrobenzoyl?oxy)propan-2-yl 3-chlorobenzoate - determined by X-ray crystal structure analysis - indicates the intermediacy of a carbenium ion during formation of the 1,2-diketones. The functionalized 1,2-diketones are valuable starting materials for a variety of products as demonstrated by the synthesis of quinoxalines, an imidazole derivative, and electron-deficient alkenes.

Dendritic Oligoglycerol Regioisomer Mixtures and Their Utility for Membrane Protein Research

Urner, Leonhard H.,Goltsche, Katharina,Selent, Marleen,Liko, Idlir,Schweder, Marc-Philip,Robinson, Carol V.,Pagel, Kevin,Haag, Rainer

supporting information, p. 2537 - 2542 (2020/12/30)

Dendrons are an important class of macromolecules that can be used for a broad range of applications. Recent studies have indicated that mixtures of oligoglycerol detergent (OGD) regioisomers are superior to individual regioisomers for protein extraction. The origin of this phenomenon remains puzzling. Here we discuss the synthesis and characterization of dendritic oligoglycerol regioisomer mixtures and their implementation into detergents. We provide experimental benchmarks to support quality control after synthesis and investigate the unusual utility of OGD regioisomer mixtures for extracting large protein quantities from biological membranes. We anticipate that our findings will enable the development of mixed detergent platforms in the future.

COMPOSITIONS AND METHODS FOR THE TREATMENT OF PARKINSON'S DISEASE

-

Page/Page column 46, (2020/05/19)

The invention relates to the compounds of formula I, formula II and/or formula III or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amount of compound of formula I, formula II or formula III, and methods for treating or preventing Parkinson's disease may be formulated for oral, buccal, rectal, topical, transdermal, transmucosal, intravenous, parenteral administration, subcutaneous, depot, intramuscular, syrup, or injection. Such compositions may be used to treatment or management of Parkinson's disease as well as scleroderma, restless leg syndrome, hypertension and gestational hypertension.

Selective monochlorination of unsymmetrical vicinal diols with chlorinated iminium chlorides

Li, Chengyang,Li, Xiaotong,Wang, Yu,Wu, Xiaoyu,Xie, Xiaomin,Yang, Liqun,Zhang, Zhaoguo

supporting information, (2020/03/23)

Chlorinated iminium chlorides have been identified to promote the highly efficient and selective mono-chlorination of unsymmetrical vicinal diols. Vilsmeier reagent, namely, (chloromethylene)dimethyliminium chloride, enables highly reactive and regioselective chlorination of 1,2- and 1,3-diols featured one secondary benzylic hydroxy group and one primary aliphatic hydroxy group to give the corresponding 1,2- and 1,3-chlorohydrins. Viehe's salts (α,α-dichloro iminium salts) exhibit excellent reactivity and good selectivity for vicinal diols to give the corresponding chlorohydrin carbamates via a cyclic intermediate in situ. The chlorination protocols tolerate diverse functional groups, including halogens, naphthalene rings, nitro, and cyano. Moreover, the optical purity of chiral diols could be retained during this chlorination reaction.

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