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BIS-(IMIDAZOL-2-YL)-METHANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64269-81-4

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64269-81-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64269-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,6 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64269-81:
(7*6)+(6*4)+(5*2)+(4*6)+(3*9)+(2*8)+(1*1)=144
144 % 10 = 4
So 64269-81-4 is a valid CAS Registry Number.

64269-81-4SDS

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 BIS-(IMIDAZOL-2-YL)-METHANE

1.2 Other means of identification

Product number -
Other names 1H,1'H-2,2'-methanediyl-bis-imidazole

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:64269-81-4 SDS

64269-81-4Downstream Products

64269-81-4Relevant academic research and scientific papers

Synthesis, characterization, structure, molecular modeling studies and biological activity of sterically crowded Pt(II) complexes containing bis(imidazole) ligands

Ravera, Mauro,Gabano, Elisabetta,Sardi, Manuele,Ermondi, Giuseppe,Caron, Giulia,McGlinchey, Michael J.,Müller-Bunz, Helge,Monti, Elena,Gariboldi, Marzia B.,Osella, Domenico

, p. 400 - 409 (2011)

The syntheses, structures and biological evaluation of a series of cisplatin-like complexes containing bis(imidazole) derivatives - the so-called Joseph ligands - are described. Their cytotoxicity is discussed in terms of their polar surface area, rate of aquation, and lipophilicity. The X-ray crystal structure of the platinum diiodido derivative of dimethyl 2-(di(1H-imidazol-2- yl)methyl)malonate) is reported and compared to those of related systems. Molecular modeling studies are focused on the hydrogen bonding properties of such systems, and their relevance to antitumor activity.

Intramolecular Imidazole-Promoted General-Base Catalysis of the Hydrolysis of an Acetylimidazole

Brown, R.S.,Clewley, R.G

, p. 1216 - 1218 (2007/10/02)

Intramolecular general-base catalysis of the hydrolysis of an acetylimidazole by imidazole is assessed by studying the hydrolysis of 2-(imidazol-2-ylmethyl)-N-acetylimidazole (3).The pH vs. log kobsd profile exhibits three major domains that consist of H2O attack on the protonated acetylimidazolium unit,OH- attack on the neutral material, and an intramolecular general-base catalysis of H2O on the neutral species.Consistent with the latter is a plateau observed in the pH profile (k3 = 1.02*10-3 s-1) at neutrality and a solvent kinetic isotope effect of kH2O/kD2O = 2.8 in that region.The effective molarity of the intramolecular imidazole in 3 can be assessed by comparing the value of k3 with the second-order rate constant for 2-methylimidazole catalyzing the hydrolysis of 2-methyl-N-acetylimidazole (4).After the difference in the imidazole pKa values is corrected for, the effective molarity of the intramolecular catalyst is 3 M.

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