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31083-15-5

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31083-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31083-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31083-15:
(7*3)+(6*1)+(5*0)+(4*8)+(3*3)+(2*1)+(1*5)=75
75 % 10 = 5
So 31083-15-5 is a valid CAS Registry Number.

31083-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxyphenyltrifluoracetat

1.2 Other means of identification

Product number -
Other names o-Methoxyphenyltrifluoracetat

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:31083-15-5 SDS

31083-15-5Relevant articles and documents

Total synthesis of "Aliskiren": The first renin inhibitor in clinical practice for hypertension

Hanessian, Stephen,Guesne, Sebastien,Chenard, Etienne

supporting information; scheme or table, p. 1816 - 1819 (2010/09/16)

We report a "macrocycle route" toward aliskiren, a drug presently marketed for the treatment of hypertension, using a highly stereocontrolled approach starting from a common "isopropyl chiron". Highlights of the synthesis include a challenging RCM reaction to produce a nine-membered unsaturated lactone, a highly stereoselective catalytic Du Bois aziridination, and a regio- and diastereoselective aziridine ring-opening to a vicinal amino alcohol.

OXIDATION BY THE SALTS OF METALS. VII. PLUMBATION AND OXIDATIVE SUBSTITUTION OF AROMATIC COMPOUNDS IN THE LEAD TETRAACETATE-LITHIUM CHLORIDE SYSTEM IN THE PRESENCE OF PERFLUORINATED CARBOXYLIC ACIDS

Serguchev, Yu. A.,Davydova, V. G.,Makhon'kov, D. I.,Beletskaya, I. P.

, p. 1006 - 1011 (2007/10/02)

The oxidation of benzene and substituted benzenes PhX with electron-donating (X = CH3, OCH3) and electron-withdrawing (X = Hlg, CF3, NO2) substituents in the Pb(OAc)4-LiCl system was investigated in the presence of perfluorinated carboxylic acids RfCOOH (Rf = CF3, C6F13).The reaction leads to the plumbation, chlorination, and acyloxylation products.It was shown that the reactions take place through the formation of aryl derivatives of lead(IV) with the participation of mixed-ligand complexes of lead.The products from the plumbation of toluene (in C6F13COOH in the absence of lithium chloride) and benzotrifluoro were isolated.In trifluoroacetic acid these intermediates undergo intramolecular redox decomposition with ligand transfer.The halogenobenzenes and benzotrifluoride are oxidized selectively in the CF3COOH-Pb(IV)-LiCl system, giving the corresponding aryl chlorides with yields close to quantitative (80-90percent).

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