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Furan, 2-[[(2-bromophenyl)sulfinyl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114325-55-2

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114325-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114325-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,2 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114325-55:
(8*1)+(7*1)+(6*4)+(5*3)+(4*2)+(3*5)+(2*5)+(1*5)=92
92 % 10 = 2
So 114325-55-2 is a valid CAS Registry Number.

114325-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-bromophenyl)sulfinylmethyl]furan

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:114325-55-2 SDS

114325-55-2Relevant academic research and scientific papers

Scope of Tandem Cycloaddition/Radical Cyclization Methodology

Ghosh, Tirthankar,Hart, Harold

, p. 5073 - 5085 (2007/10/02)

Tandem cycloaddition/radical cyclization is an effective strategy for the rapid assembly of a wide variety of ring systems.To set up the reagents for this sequence, it is necessary to include a potential radical site in one of the two cycloaddition partners, located at an appropriate distance from a new double bond that will be formed in the cycloaddition step.Examples in which the cycloaddition step is or and in which the radical cyclization creates 5-, 6-, or 7-membered rings are described.Examples of the tandem methodology carried out in a completely intramolecular mode are also described.

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