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85353-80-6

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85353-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85353-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,5 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85353-80:
(7*8)+(6*5)+(5*3)+(4*5)+(3*3)+(2*8)+(1*0)=146
146 % 10 = 6
So 85353-80-6 is a valid CAS Registry Number.

85353-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phytyl-3,5,6-trimethylhydroquinone

1.2 Other means of identification

Product number -
Other names PTMHQ

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:85353-80-6 SDS

85353-80-6Relevant articles and documents

Friedel-Crafts alkylations on nanoscopic inorganic fluorides

Candu,Wuttke,Kemnitz,Coman,Parvulescu

experimental part, p. 169 - 174 (2011/10/05)

The catalytic potential of nanoscopic MFx (M = Mg, Al; x = 2, 3) has been investigated using batch Friedel-Crafts alkylation of aromatic compounds, including benzene, ethylbenzene, trimethylhydroquinone (TMHQ), and menadiol (MDL), with isophytol and benzyl alcohol. The conversion of isophytol was 100% in the reactions with trimethylhydroquinone (TMHQ), menadiol (MDL) and benzene while the highest selectivity in alkylated compounds was achieved with TMHQ (>99%). The different reaction rates of the alkylation reactions are due to the different nucleophylicities of the substrates, and therefore, due to their ability to delocalize the positive charge in the Wheland intermediate by inductive and resonance effects. The conversions of benzyl alcohol varied between 10 and 84% as a function of the catalyst nature and reaction conditions while the highest selectivity to monobenzyl derived compounds (25%) was achieved with ethylbenzene. The formation of high amounts of dibenzyl ether was also observed, indicating the presence of high amounts of Br?nsted acid sites in this type of catalysts.

PROCESS FOR THE MANUFACTURE OF ALKENYLATED HYDROXYLATED AROMATIC COMPOUNDS, OF CHROMAN COMPOUNDS AND OF THEIR ACYLATED DERIVATIVES

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Page/Page column 37, (2008/06/13)

The present invention relates to a novel process for the manufacture of alkenylated aro-matic compounds featuring at least one hydroxy group, their ring-closure reactions to chroman derivatives, as well as the acylation of the latter and the aromatic compounds featuring at least one hydroxy group themselves. The present invention relates especially to a process for the manufacture of tocol, tocopherols and their alkanoates such as α-tocopherol (TCP) and alkanoates (TCPA) thereof, preferably α-tocopheryl acetate (TCPAc). The processes of the present invention are characterized in that at least one step of the processes is carried out in the presence of an indium salt as the catalyst. Thus, an object of the present invention is the use of an indium salt as the catalyst in Friedel-Crafts alkylation reactions of aromatic compounds featuring at least one hydroxy group and ring-closure reactions of the latter to produce chroman-ring compounds in organic solvents. According to another aspect of the invention indium salts can be used as the catalyst in processes for the manufacture of tocyl alkanoates, tocopheryl alkanoates and alkanoates of aromatic compounds featuring at least one hydroxy group by reacting tocols, tocopherol and aromatic compounds featuring at least one hydroxy group, respectively, with an acylating agent. Suitable indium salts are indium(III) salts, especially indium trichloride, indium tribromide or indium triiodide, indium(III) triflate, indium(III) bis(trifluoromethanesulfonamide) and indium(III) acetate. In preferred embodiments of the invention the processes are carried out at a pressure of at least 0.96 bar, whereby the acylation can be carried out at an absolute pressure of at least 0.02 bar.

Tocopherols, tocotrienols, other chroman and side chain derivatives and uses thereof

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Page column Sheet 8; 36, (2008/06/13)

The present invention provides an antiproliferative compound having a structural formula where X and Y independently are oxygen, nitrogen o r sulfur; R1 is alkyl, alkenyl, alkynyl, aryl, heteroaryl, carboxylic acid, carboxylate, carboxamide, ester, thioamide, thiolacid, thiolester, saccharide, alkoxy-linked saccharide, amine, sulfonate, sulfate, phosphate, alcohol, ethers or nitriles; R2 and R3 are hydrogen or R4; R4 is methyl, benzyl carboxylic acid, benzyl carboxylate, benzyl carboxamide, benzylester, saccharide or amine; and R5 is alkenyl; where when Y is nitrogen, said nitrogen is substituted with R6, wherein R6 is hydrogen or methyl. Also provided are methods for treating a cell proliferative disease and for inducing apoptosis in a cell comprising administering this compound is also provided.

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