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Benzene, 1,1'-methylenebis[2,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10259-11-7

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10259-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10259-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,5 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10259-11:
(7*1)+(6*0)+(5*2)+(4*5)+(3*9)+(2*1)+(1*1)=67
67 % 10 = 7
So 10259-11-7 is a valid CAS Registry Number.

10259-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2,6-dimethylphenyl)methane

1.2 Other means of identification

Product number -
Other names Bis-(2,6-dimethyl-phenyl)-methan

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:10259-11-7 SDS

10259-11-7Downstream Products

10259-11-7Relevant academic research and scientific papers

One-pot synthesis of symmetrical and unsymmetrical diarylmethanes via diborylmethane

Endo, Kohei,Ishioka, Takafumi,Ohkubo, Takahiro,Shibata, Takanori

, p. 7223 - 7231 (2012/10/29)

A one-pot synthesis of diarylmethanes from air-stable diborylmethane via the Suzuki-Miyaura cross-coupling reaction is described. The present approach realizes the synthesis of various symmetrical and unsymmetrical diarylmethanes in good to excellent yields.

Spectroscopic and product studies of the effect of para substituents on the reactivity of triplet bis(2,6-dimethylphenyl)carbenes

Hu, Yingmo,Ishikawa, Yui,Hirai, Katsuyuki,Tomioka, Hideo

, p. 2207 - 2218 (2007/10/03)

A series of diazobis(2,6-dimethylphenyl)methanes (1) bearing eight symmetrical para di-substituents have been prepared and photolyzed to generate the corresponding carbenes (2). Product analysis studies showed that carbenes (2) decay mainly either by dimerization to form tetra(aryl)ethylene (3) or by attack at an o-methyl group to afford 1,2-dihydrobenzocyclobutenes (4) by way of o-quinodimethanes (6) in solution. The zero-field splitting parameters, D and E, were measured in matrices of different viscosities and are analyzed in terms of a sigma-dot (σ.) scale of spin-delocalization substituent constants. Fairly good correlation with σ. was found for the D values of 32 in its minimum energy geometry. Stabilities of 32 were estimated either by measuring the temperature at which the triplet carbene signals disappeared upon thawing the matrix or by analyzing the decay kinetics of 32 in a degassed solution at room temperature. They are examined in terms of the D values in matrix at low temperature and in terms of product distributions in solution at room temperature.

Diamino compounds and methods for preparing them

-

, (2008/06/13)

An object of the invention is to propose diamino compounds expressed by the following general formula (1) which are suitable to obtain a raw material, a polyimide resin, for a liquid crystal aligning film without any image sticking and with a high voltage holding ratio at from a low temperature to a high temperature as well as the preparation thereof: STR1

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