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2-(2,4,6-trimethoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

335343-08-3

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335343-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335343-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,3,4 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 335343-08:
(8*3)+(7*3)+(6*5)+(5*3)+(4*4)+(3*3)+(2*0)+(1*8)=123
123 % 10 = 3
So 335343-08-3 is a valid CAS Registry Number.

335343-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-2-(2,4,6-trimethoxyphenyl)-1,3,2-dioxaborinane

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:335343-08-3 SDS

335343-08-3Downstream Products

335343-08-3Relevant academic research and scientific papers

Suzuki cross-coupling reaction of sterically hindered aryl boronates with 3-iodo-4-methoxybenzoic acid methylester

Chaumeil,Signorella,Le Drian

, p. 9655 - 9662 (2007/10/03)

The cross-coupling reaction of 3-iodo-4-methoxybenzoic acid methylester with sterically hindered arylboronic esters and especially 5,5-dimethyl-2-mesityl-1,3,2-dioxaborinane, is reported. The optimisation of the process in order to obtain biaryls in good yield by using anhydrous benzene at reflux and sodium phenoxide in the presence of 0.06 equiv. of Pd(PPh3)4 is described. (C) 2000 Elsevier Science Ltd.

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