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6364-27-8

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6364-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6364-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6364-27:
(6*6)+(5*3)+(4*6)+(3*4)+(2*2)+(1*7)=98
98 % 10 = 8
So 6364-27-8 is a valid CAS Registry Number.

6364-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-p-tolyl-m-phenetidine

1.2 Other means of identification

Product number -
Other names m-Ethoxy-N-phenylcarbanilic acid 2-(dimethylamino)ethyl ester

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:6364-27-8 SDS

6364-27-8Relevant articles and documents

Synthesis of oxygenated carbazoles by palladium-mediated oxidative double C-H activation of diarylamines assisted by microwave irradiation

Sridharan, Vellaisamy,Martín, Ma. Antonia,Menéndez, J. Carlos

, p. 2375 - 2378 (2008/02/09)

Microwave irradiation in the presence of palladium acetate and traces of dimethylformamide allows the fast and efficient cyclodehydrogenation of diphenylamines into carbazoles. The scope of the microwave-assisted reaction is broader than that of the one using conventional conditions in that it allows the preparation of oxygenated carbazoles without apparent loss in yield. The applicability of the method to the preparation of carbazole alkaloids has been demonstrated by the development of a total synthesis of murrayafoline A, which proceeds in 50% overall yield from commercially available materials and is the shortest and most efficient route for the preparation of this alkaloid to date. Georg Thieme Verlag Stuttgart.

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