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1,8-Naphthyridine, 7-(diphenylphosphino)-2,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144101-82-6

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144101-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144101-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,0 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144101-82:
(8*1)+(7*4)+(6*4)+(5*1)+(4*0)+(3*1)+(2*8)+(1*2)=86
86 % 10 = 6
So 144101-82-6 is a valid CAS Registry Number.

144101-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5,7-dimethyl-1,8-naphthyridin-2-yl)-diphenylphosphane

1.2 Other means of identification

Product number -
Other names 7-diphenylphosphino-2,4-dimethyl-1,8-naphthyridine

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:144101-82-6 SDS

144101-82-6Relevant academic research and scientific papers

Polyfunctional Phosphine Ligands. Synthesis of 7-Diphenylphosphino-2,4-dimethyl-1,8-naphthyridine and its Co-ordination Properties

Grassi, Maria,Munno, Giovanni De,Nicolo, Francesco,Schiavo, Sandra Lo

, p. 2367 - 2374 (1992)

The new trinucleating ligand 7-diphenylphosphino-2,4-dimethyl-1,8-naphthyridine (dpnapy) has been prepared and its co-ordination chemistry with rhodium(I) complexes investigated.Reactions with 2> (cod = cycloocta-1,5-diene) lead to different products depending on the ligand to metal ratio.The P-monodentate ligand complex 1 is formed when a 2:1 ligand:dimer ratio is used.The cod region of the 1H and 13C NMR spectra of 1 is temperature dependent.The fluxional behaviour can be explained by the formation of a five-co-ordinate intermediate displaying rapid intramolecular exchange of the cod olefinic and CH2 protons.A lower activation energy process, not frozen at 215 K, is also observed.At room temperature (r.t.) the two-dimensional 1H and 31P chemical exchange spectra indicate a further slower dynamic equilibrium 1 2 with loss of dpnapy.The binuclear complex 2(μ-dpnapy)> 2, in which dpnapy acts as bridging bidentate ligand using the phosphorus and the terminal nitrogen atoms, is the reaction product when a 1:1 ligand:dimer ratio is used.The 1H and 13C NMR data for complex 2 are consistent with a dimeric structure of low symmetry.Complex 2 is also involved in several dynamic processes.At r.t. the two-dimensional 1H chemical exchange spectrum shows a slow general scrambling of the cod olefinic protons and the presence of the equilibrium 2 1 with participation of 2>.The ligand reacts with 2> giving as the only isolable product the metallocycle 2>*2CH2Cl2 3.The reaction proceeds through several steps involving the formation of cis-dicarbonyl intermediates as indicated by IR and NMR spectra.The structure of 3 has been determined by X-ray crystallography.It consists of two Rh(CO)Cl units, joined together by two dpnapy molecules in a head-to-tail arrangement.

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