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3367-51-9

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3367-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3367-51-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3367-51:
(6*3)+(5*3)+(4*6)+(3*7)+(2*5)+(1*1)=89
89 % 10 = 9
So 3367-51-9 is a valid CAS Registry Number.

3367-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(4-methoxyphenyl)piperazine

1.2 Other means of identification

Product number -
Other names -

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:3367-51-9 SDS

3367-51-9Downstream Products

3367-51-9Relevant articles and documents

Copper-Catalyzed para-Selective C-H Amination of Electron-Rich Arenes

Berzina, Beatrise,Sokolovs, Igors,Suna, Edgars

, p. 7008 - 7014 (2015/11/23)

A one-pot two-step method for para-selective C-H amination of carbocyclic arenes comprises the in situ formation of unsymmetrical diaryl-λ3-iodanes followed by their Cu(I)-catalyzed reaction with a range of N-unprotected amines.

Nickel-mediated amination chemistry. Part 2: Selective N-arylation or N,N'-diarylation of piperazine

Brenner, Eric,Schneider, Rapha?l,Fort, Yves

, p. 2881 - 2884 (2007/10/03)

The 2,2'-bipyridine liganded Ni catalyst has revealed a good selectivity in the mono arylation of piperazine starting from aryl chlorides allowing a selective and efficient synthesis of N-arylpiperazines using stoichiometric amounts of reagents. The preparation of N,N'-diaryl substituted piperazines is also described. (C) 2000 Elsevier Science Ltd.

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