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Boronic acid, B-[2-bromo-5-(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

916747-52-9

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916747-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916747-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,7,4 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 916747-52:
(8*9)+(7*1)+(6*6)+(5*7)+(4*4)+(3*7)+(2*5)+(1*2)=199
199 % 10 = 9
So 916747-52-9 is a valid CAS Registry Number.

916747-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-5-tert-butylphenyl)boronic acid

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:916747-52-9 SDS

916747-52-9Downstream Products

916747-52-9Relevant academic research and scientific papers

Oligoindenopyrenes: A new class of polycyclic aromatics

Wegner, Hermann A.,Reisch, Helge,Rauch, Karsten,Demeter, Attila,Zachariasse, Klaas A.,De Meijere, Armin,Scott, Lawrence T.

, p. 9080 - 9087 (2007/10/03)

(Graph Presented) A new class of polycyclic aromatic hydrocarbons - oligoindenopyrenes - has been synthesized featuring a Pd-catalyzed Suzuki - Heck coupling cascade. The oligoindenopyrenes are robust, highly colored substructures of C70 and have properties that might prove useful in new organic materials or devices. After excitation, the tetraindenopyrene derivative 3d undergoes efficient deactivation (99%) by internal conversion to the ground state. The small fluorescence quantum yield (0.004) is in accordance with the short (0.6 ns) fluorescence decay time.

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