156150-67-3 Usage
Chemical Properties
Clear colourless to light yellow liquid
Uses
Different sources of media describe the Uses of 156150-67-3 differently. You can refer to the following data:
1. 3-Chloro-4-Fluoroiodobenzene can be used as CDK2 inhibitors for enzyme inhibitory activity.
2. 3-Chloro-4-fluoroiodobenzene may be used in the preparation of 2-chloro-1-(3,5-dimethoxyphenoxy)-4-iodobenzene by reacting with 3,5-dimethoxyphenol in the presence of cesium carbonate.
General Description
3-Chloro-4-fluoroiodobenzene, also known as 2-chloro-1-fluoro-4-iodobenzene [IUPAC name], is a polyhalobenzene. It participates in the synthesis of 3-carboxythiophene analogs.
Check Digit Verification of cas no
The CAS Registry Mumber 156150-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,5 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 156150-67:
(8*1)+(7*5)+(6*6)+(5*1)+(4*5)+(3*0)+(2*6)+(1*7)=123
123 % 10 = 3
So 156150-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClFI/c7-5-2-1-4(9)3-6(5)8/h1-3H
156150-67-3Relevant articles and documents
Direct Transformation of Arylamines to Aryl Halides via Sodium Nitrite and N-Halosuccinimide
Mukhopadhyay, Sushobhan,Batra, Sanjay
supporting information, p. 14622 - 14626 (2018/09/21)
A one-pot universal approach for transforming arylamines to aryl halides via reaction with sodium nitrite (NaNO2) and N-halosuccinimide (NXS) in DMF at room temperature under metal- and acid-free condition is described. This new protocol that is complementary to the Sandmeyer reaction, is suggested to involve the in situ generation of nitryl halide induce nitrosylation of aryl amine to form the diazo intermediate which is halogenated to furnish the aryl halide.