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Benzene, (3-iodoheptyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80471-71-2

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80471-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80471-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80471-71:
(7*8)+(6*0)+(5*4)+(4*7)+(3*1)+(2*7)+(1*1)=122
122 % 10 = 2
So 80471-71-2 is a valid CAS Registry Number.

80471-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-iodo-1-phenylheptane

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-iodoheptane

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:80471-71-2 SDS

80471-71-2Relevant academic research and scientific papers

Synthesis of Nitrile-Bearing Quaternary Centers by an Equilibrium-Driven Transnitrilation and Anion-Relay Strategy

Alazet, Sébastien,West, Michael S.,Patel, Purvish,Rousseaux, Sophie A. L.

supporting information, p. 10300 - 10304 (2019/07/04)

The efficient preparation of nitrile-containing building blocks is of interest due to their utility as synthetic intermediates and their prevalence in pharmaceuticals. As a result, significant efforts have been made to develop methods to access these motifs which rely on safer and non-toxic sources of CN. Herein, we report that 2-methyl-2-phenylpropanenitrile is an efficient, non-toxic, electrophilic CN source for the synthesis of nitrile-bearing quaternary centers by a thermodynamic transnitrilation and anion-relay strategy. This one-pot process leads to nitrile products resulting from the gem-difunctionalization of alkyl lithium reagents.

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