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Mercury, chloro[2-(2-pyridinyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106995-39-5

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106995-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106995-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,9 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106995-39:
(8*1)+(7*0)+(6*6)+(5*9)+(4*9)+(3*5)+(2*3)+(1*9)=155
155 % 10 = 5
So 106995-39-5 is a valid CAS Registry Number.

106995-39-5SDS

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 chloro-(2-pyridin-2-ylphenyl)mercury

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:106995-39-5 SDS

106995-39-5Relevant academic research and scientific papers

Cyclometallated gold(III) complexes as effective catalysts for synthesis of propargylic amines, chiral allenes and isoxazoles

Kung, Karen Ka-Yan,Lo, Vanessa Kar-Yan,Ko, Hok-Ming,Li, Gai-Li,Chan, Pui-Ying,Leung, King-Chi,Zhou, Zhongyuan,Wang, Ming-Zhong,Che, Chi-Ming,Wong, Man-Kin

, p. 2055 - 2070 (2013/08/23)

A series of cyclometallated gold(III) complexes [Au(CN)Cl2] 1a-l (HCN=arylpyridines) and a PEG-linked complex 1m were synthesized. Complexes 1a-m are effective in catalyzing the synthesis of propargylic amines, chiral allenes and isoxazoles. Six-membered ring cyclometallated gold(III) complexes 1f-l exhibited higher catalytic activity than five-membered ring cyclometallated gold(III) complexes 1a-e. The diastereoselectivity of propargylic amines could be tuned by using chiral aldehyde and/or amine substrates. Excellent enantioselectivities (90-98% ee) were achieved in chiral allene synthesis. Chiral allene racemization could be minimized by using 1f as catalyst. The PEG-linked catalyst 1m is the most catalytically active towards synthesis of propargylic amines, in which case a product turnover of 900 was achieved. Moreover, 1m could be repeatedly used for 12 reaction cycles, leading to an overall turnover number of 872. Copyright

Mercury(II) and gold(III) derivatives of 2-phenyl pyridines and 2-phenyl-4-(methylcarboxylato)quinoline

Parish,Wright, Jonathan P.,Pritchard, Robin G.

, p. 165 - 176 (2007/10/03)

ortho-Mercurated derivatives of several substituted 2-phenylpyridines and of 2-phenyl-4-(methylcarboxylato)quinoline have been prepared and characterised. C,N-chelated gold(III) derivatives, [AuCl2(C6H4C5H3RN)] (R = H, 3-Me, 3,5-Me2, 4-Prn, 4-But) are prepared more efficiently by trans-metallation reactions than by direct reaction of AuCl4- with the phenylpyridines. The new gold complexes were characterised spectroscopically and a variety of substitution reactions have been effected. As is usual with unsymmetrical bidentate ligands, the softer donor atom is found trans to the N-donor of the pyridine unit. Crystal-structure determinations are reported for [Au(OAc)(pmpy)(py)]ClO4, [Au(ppy)(dpbt)]BPh4, [Au(ppy)(S2CNMe2)]BPh4 and AuCl(pqcm)2 [Hppy = 2-phenylpyridine, Hpmpy = 2-phenyl-3-methylpyridine, Hpqcm = 2-phenyl-4-(methylcarboxylato)quinoline].

2-Pyridyl- and Quinolin-2-yl-functionalised Organyltellurium Ligands. The Stabilisation of Diorganyl Tritellurides. The Crystal and Molecular Structures of 2-(2-Pyridyl)phenyltellurium(IV) Tribromide, Dimethyldithiocarbamatotellurium(

Al-Salim, Najih,West, Antony A.,McWhinnie, William R.,Hamor, Thomas A.

, p. 2363 - 2372 (2007/10/02)

The syntheses and spectroscopic data (13C n.m.r.) for some new organyltellurium ligands are described.Thus trans metallation of 2-(2-pyridyl)phenyl- (R) or 2-(quinolin-2-yl)phenyl- (R') mercury(II) chloride with TeBr4 gives the organyltellurium tribromide

BIS(2-(2-PYRIDYL)PHENYL)TRITELLURIDE - SYNTHESIS AND CRYSTAL STRUCTURE

Hamor, Thomas A.,Al-Salim, Najih,West, Antony A.,Mcwhinnie, William R.

, p. C5 - C7 (2007/10/02)

The synthesis and molecular structure of bis(2-(2-pyridyl)phenyl)tritelluride are described.There is a short Te...N non-bonded interaction of 2.554(7) Angstroem, which may be responsible for the stability of the molecule.The tritelluride can be converted

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