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Benzenamine, 4-[bis(2,4,6-trimethylphenyl)boryl]-N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38186-30-0

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38186-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38186-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38186-30:
(7*3)+(6*8)+(5*1)+(4*8)+(3*6)+(2*3)+(1*0)=130
130 % 10 = 0
So 38186-30-0 is a valid CAS Registry Number.

38186-30-0SDS

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 4-bis(2,4,6-trimethylphenyl)boranyl-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4-(dimesitylboryl)-N,N-dimethylaniline

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:38186-30-0 SDS

38186-30-0Downstream Products

38186-30-0Relevant academic research and scientific papers

Direct Introduction of a Dimesitylboryl Group Using Base-Mediated Substitution of Aryl Halides with Silyldimesitylborane

Yamamoto, Eiji,Izumi, Kiyotaka,Shishido, Ryosuke,Seki, Tomohiro,Tokodai, Noriaki,Ito, Hajime

, p. 17547 - 17551 (2016/11/28)

The first dimesitylboryl substitution of aryl halides with a silylborane bearing a dimesitylboryl group in the presence of alkali-metal alkoxides is described. The reactions of aryl bromides or iodides with Ph2MeSi?BMes2and Na(OtBu) afforded the desired aryl dimesitylboranes in good to high yields and with high borylation/silylation ratios. Selective reaction of the sterically less-hindered C?Br bond of dibromoarenes provided monoborylated products. This reaction was used to rapidly construct a D-π-A aryl dimesityl borane with a non-symmetrical biphenyl spacer.

Synthesis, crystal structures, linear and nonlinear optical properties, and theoretical studies of (p-R-phenyl)-, (p-R-phenylethynyl)-, and (E)-[2-(p-Rphenyl)ethenyl]dimesitylboranes and related compounds

Yuan, Zheng,Entwistle, Christopher D.,Collings, Jonathan C.,Albesa-Jove, David,Batsanov, Andrei S.,Howard, Judith A. K.,Taylor, Nicholas J.,Kaiser, Hanns Martin,Kaufmann, Dieter E.,Poon, Suk-Yue,Wong, Wai-Yeung,Jardin, Christophe,Fathallah, Sofiane,Boucekkine, Abdou,Halet, Jean-Francois,Marder, Todd B.

, p. 2758 - 2771 (2008/02/03)

The (p-R-phenyl)dimesitylboranes (R = Me2N, MeO, MeS, Br, I), (p-R-phenylethynyl)dimesitylboranes (R = Me2N, MeO, MeS, H), (E)-[2-(pR-phenyl)ethenyl]dimesitylboranes (R = Me2N, H2N, MeO, MeS, H, CN, NO2/su

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