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1,3-Dioxolane, 4-[[(3,4-dimethoxyphenyl)methoxy]methyl]-2,2-dimethyl-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139115-86-9

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139115-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139115-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139115-86:
(8*1)+(7*3)+(6*9)+(5*1)+(4*1)+(3*5)+(2*8)+(1*6)=129
129 % 10 = 9
So 139115-86-9 is a valid CAS Registry Number.

139115-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-4-{[(3,4-Dimethoxybenzyl)oxy]methyl}-2,2-dimethyl-1,3-dioxol ane

1.2 Other means of identification

Product number -
Other names 4-methyl-1-octyn-4-ol trimethylsilyl ether

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:139115-86-9 SDS

139115-86-9Relevant academic research and scientific papers

Synthesis and properties of photoactivatable phospholipid derivatives designed to probe the membrane-associate domains of proteins

Alcaraz, Marie-Lyne,Peng, Ling,Klotz, Philippe,Goeldner, Maurice

, p. 192 - 201 (1996)

The total syntheses of photoactivatable phospholipidic probes 1 and 2 are described. These probes contain either an aryldiazonium function at their polar head (probes 1a and 1b) or an diazocyclohexadienonyl group attached to the end of one fatty acid side chain (probe 2) and have been designed to probe the lipid/water interface and the hydrophobic core of the membrane, respectively. The synthetic schemes include the possibility of incorporating a radio-labeled atom (tritium) for further labeling investigations. Both probes were stable in the dark under physiological conditions and could be efficiently photodecomposed at wavelengths above 300 nm, leading to the generation of highly reactive species, aryl cations and cyclohexadienonyl carbene, respectively. In addition, these probes displayed UV-absorption spectra which are compatible with tryptophan-mediated energy transfer photoactivation, which can lead potentially to an efficient mapping of the membrane-associate protein domains.

Identification of CDP-archaeol synthase, a missing link of ether lipid biosynthesis in Archaea

Jain, Samta,Caforio, Antonella,Fodran, Peter,Lolkema, Juke S.,Minnaard, Adriaan J.,Driessen, Arnold J.M.

supporting information, p. 1392 - 1401 (2014/12/11)

Archaeal membrane lipid composition is distinct from Bacteria and Eukarya, consisting of isoprenoid chains etherified to the glycerol carbons. Biosynthesis of these lipids is poorly understood. Here we identify and characterize the archaeal membrane prote

Synthesis of New Phospholipids Linked to Steroid-Hormone Derivatives Designed for Two-Dimensional Crystallization of Proteins

Lebeau, Luc,Oudet, Pierre,Mioskowski, Charles

, p. 1697 - 1706 (2007/10/02)

The synthesis of phospholipids 1n-3n, rationally designed for two-dimensional crystallization of progesterone and estradiol receptors, is reported.The structure of theses lipids provides them with essential properties such as fluidity and stability when spread into monolayers at the air/H2O interface, affinity for the protein to be crystallized, and accessibility of the ligand under the lipid monolayer.

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