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68258-04-8

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68258-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68258-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68258-04:
(7*6)+(6*8)+(5*2)+(4*5)+(3*8)+(2*0)+(1*4)=148
148 % 10 = 8
So 68258-04-8 is a valid CAS Registry Number.

68258-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-phenylbenzeneamine oxide

1.2 Other means of identification

Product number -
Other names Methyldiphenylamin-N-oxid

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:68258-04-8 SDS

68258-04-8Relevant articles and documents

Oxygen Atom Transfer to Cationic PCPNi(II) Complexes Using Amine-N-Oxides

LaPierre, Etienne A.,Clapson, Marissa L.,Piers, Warren E.,Maron, Laurent,Spasyuk, Denis M.,Gendy, Chris

supporting information, p. 495 - 506 (2018/01/10)

Three PCsp3P pincer ligands differing in the aryl group linking the phosphine arms with the anchoring carbon donor were used to support square planar Ni(II) bromide complexes 1-3Br. Exchange of the coordinating bromide anion for the

Deoxygenation of tertiary amine N-oxides under metal free condition using phenylboronic acid

Gupta, Surabhi,Sureshbabu, Popuri,Singh, Adesh Kumar,Sabiah, Shahulhameed,Kandasamy, Jeyakumar

supporting information, p. 909 - 913 (2017/02/15)

A simple and efficient method for the deoxygenation of amine N-oxides to corresponding amines is reported using the green and economical reagent phenylboronic acid. Deoxygenation of N,N-dialkylaniline N-oxides, trialkylamine N-oxides and pyridine N-oxides were achieved in good to excellent yields. The reduction susceptible functional groups such as ketone, amide, ester and nitro groups are well tolerated with phenylboronic acid during the deoxygenation process even at high temperature. In addition, an indirect method for identification and quantification of tert-amine N-oxide is demonstrated using UV–Vis spectrometry which may be useful for drug metabolism studies.

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