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N,N-bis(pyrimid-2-yl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

334977-67-2

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334977-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334977-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,9,7 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 334977-67:
(8*3)+(7*3)+(6*4)+(5*9)+(4*7)+(3*7)+(2*6)+(1*7)=182
182 % 10 = 2
So 334977-67-2 is a valid CAS Registry Number.

334977-67-2SDS

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,N-bis(pyrimid-2-yl)amine

1.2 Other means of identification

Product number -
Other names bis(pyrimidin-2-yl)amine

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:334977-67-2 SDS

334977-67-2Downstream Products

334977-67-2Relevant academic research and scientific papers

Bis(pyrimidine)-based palladium catalysts: Synthesis, X-ray structure and applications in Heck-, Suzuki-, Sonogashira-Hagihara couplings and amination reactions

Buchmeiser, Michael R.,Schareina, Thomas,Kempe, Rhett,Wurst, Klaus

, p. 39 - 46 (2001)

The synthesis of N,N-bis(pyrimid-2-yl)amine (1), N-acetyl-N,N-bis(pyrimid-2-yl)amide (2), N-norborn-2-ene-5-ylbis(pyrimid-2-yl)carbamide (4) is described. The Pd-complex N-acetyl-N,N-bis(pyrimid-2-yl)amine palladium dichloride (3) has been prepared from compound 2 and its X-ray structure has been determined. A polymer supported catalytic system (6) was prepared via ring-opening metathesis copolymerization of 4 with 1,4,4a,5,8,8a-hexahydro-1,4,5,8-exo-endo-dimethanonaphthalene (HDMN-6) and subsequent loading with PdCl2. Both the homogeneous and heterogeneous catalysts 3 and 6 were active in Heck-, Suzuki-, Sonogashira-Hagihara-type couplings and amination reactions using aryl iodides, bromides and chlorides.

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