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Methanimidamide, N,N'-bis(pentafluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68090-77-7

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68090-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68090-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,9 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68090-77:
(7*6)+(6*8)+(5*0)+(4*9)+(3*0)+(2*7)+(1*7)=147
147 % 10 = 7
So 68090-77-7 is a valid CAS Registry Number.

68090-77-7SDS

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,N'-bis(2,3,4,5,6-pentafluorophenyl)methanimidamide

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:68090-77-7 SDS

68090-77-7Relevant academic research and scientific papers

Reduction of CO2 by Hydrosilanes in the Presence of Formamidinates of Group 13 and 12 Elements

Dorcet, Vincent,Huang, Weiheng,Kirillov, Evgueni,Orione, Clement,Roisnel, Thierry

, (2020)

Homoleptic complexes 1-M of group 13 and 12 elements (M = B-In and M = Zn, respectively) incorporating electron-withdrawing formamidinate ligands {(C6F5)N═CHN(C6F5)}- ({NCN}-) were synthesi

Intermolecular hydrogen-fluorine interaction in dimolybdenum triply bonded complexes modified by fluorinated formamidine ligands for the construction of 2D- and 3D-networks

Krackl, Sebastian,Inoue, Shigeyoshi,Driess, Matthias,Enthaler, Stephan

experimental part, p. 2103 - 2111 (2011/07/07)

The formamidines ArNHC(H)=N-Ar [Ar = Ph (2a), 4-F-Ph (2b), 3,5-F 2Ph (2c) and 2,6-F2Ph (2d) and R = 2,3,5-F3Ph (2e), 3,4,5-F3Ph (2f), F5Ph (2g) and 4-CF3Ph (2h)] were synthesized and the influence of the introduction of a fluorine or a trifluoromethyl group into the aryl unit on the solid-state structures was investigated. On comparing the experimental data, only marginal differences in the geometrical and electronic features of the diverse substituted species were detected. DFT calculations and X-ray crystallography of 2d-2g revealed that the E-syn-configuration corresponded to the thermodynamically most stable motif of all of the examined formamidines. However, in their solid-state, these ligands showed a range of H...F interactions, which varied depending on the number and position of the fluorine atoms on the aryl group and thus led to interesting solid-state structures. Moreover, compounds 2 were used for the synthesis of the new heteroleptic dimolybdenum triply-bonded complexes, Mo 2[(2a-2c; 2e-f)-H]2(OtBu)4 (3a-3c; 3e-3f). X-ray crystallography of complexes 3c and 3f revealed two different isomers in the solid state: in trans-3c the two formamidines are in one plane, while in cis-3c and cis-3f they are next to each other. The DFT calculations showed only a small distinction in energy between the configurations, which led us to assume that the different configurations were induced by the crystal packing. The specific H...F interactions provided by the different formamidines led to a two-dimensional arrangement for trans-3c and a three-dimensional network for cis-3c and cis-3f.

Anionic N-heterocyclic carbenes with N,N′-Bis(fluoroaryl) and N,N′-bis(perfluoroaryl) substituents

Hobbs, Matthew G.,Knapp, Chrissy J.,Welsh, Patrick T.,Borau-Garcia, Javier,Ziegler, Tom,Roesler, Roland

body text, p. 14520 - 14533 (2011/03/22)

A series of rhodium complexes, [Rh(cod)(NHC-Fx)(OH2)] (cod=1,5-cyclooctadiene; NHC=N-heterocyclic carbene), incorporating anionic N-heterocyclic carbenes with 2-tert-butylmalonyl backbones and 2,6-dimethylphenyl (x=0), 2,6-difluoroph

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