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Magnesium, [3,5-bis(1,1-dimethylethyl)-4-[(trimethylsilyl)oxy]phenyl]bromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54907-62-9

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54907-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54907-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,0 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54907-62:
(7*5)+(6*4)+(5*9)+(4*0)+(3*7)+(2*6)+(1*2)=139
139 % 10 = 9
So 54907-62-9 is a valid CAS Registry Number.

54907-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,5-di-tert-butyl-4-(trimethylsiloxy)phenyl]magnesium bromide

1.2 Other means of identification

Product number -
Other names (3,5-di-tert-butyl-4-trimethylsiloxyphenyl)magnesium bromide

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:54907-62-9 SDS

54907-62-9Relevant academic research and scientific papers

Selective introducing of aryl and amino groups: Reaction of benzanthrone and organometallic reagents

Umeda, Rui,Namba, Teruaki,Yoshimura, Tomohiro,Nakatsukasa, Masamichi,Nishiyama, Yutaka

, p. 1526 - 1531 (2013/02/23)

The reaction of benzanthrone and aryl magnesium bromides produced 6-aryl-substituted benzanthrones in moderate to good yields. Similarly, 6-alkylaminobenzanthrones were selectively prepared by the reaction of benzanthrone and lithium alkylamides. In contrast, for the lithium arylamides, the arylamino groups were selectively introduced at the 4-position of the benzanthrone.

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