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4-Bromomethyl-3-fluorophenylboronic acid,pinacol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1150271-74-1

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1150271-74-1 Usage

Uses

4-Bromomethyl-3-fluorophenylboronic acid, pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 1150271-74-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,0,2,7 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1150271-74:
(9*1)+(8*1)+(7*5)+(6*0)+(5*2)+(4*7)+(3*1)+(2*7)+(1*4)=111
111 % 10 = 1
So 1150271-74-1 is a valid CAS Registry Number.

1150271-74-1SDS

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-(4-(Bromomethyl)-3-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-[4-(bromomethyl)-3-fluorophenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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:1150271-74-1 SDS

1150271-74-1Relevant academic research and scientific papers

A modular approach to catalytic synthesis using a dual-functional linker for Click and Suzuki coupling reactions

White, James R.,Price, Gareth J.,Schiffers, Stefanie,Raithby, Paul R.,Plucinski, Pawel K.,Frost, Christopher G.

supporting information; experimental part, p. 3913 - 3917 (2010/08/22)

The stable benzylazido-boronate ester 1 is presented as an example of a dual-functional linker that allows the synthetically valuable boronate motif to be clicked onto other molecules under mild conditions. The utility of the azido-boronate motif as a modular building block is demonstrated in the rapid synthesis of drug-like structures employing sequential catalytic azide-alkyne cycloaddition and Suzuki coupling reactions.

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