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tert-butyl 2-(4-chlorophenoxy)-2-methylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124188-31-4

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124188-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124188-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,8 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124188-31:
(8*1)+(7*2)+(6*4)+(5*1)+(4*8)+(3*8)+(2*3)+(1*1)=114
114 % 10 = 4
So 124188-31-4 is a valid CAS Registry Number.

124188-31-4Relevant academic research and scientific papers

PROTEIN-PROTEIN INTERACTION STABILIZERS

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Paragraph 0860-0861, (2021/10/11)

Provided herein, inter alia, are stabilizers of protein-protein interactions and methods of identifying and using the same.

Site-Directed Fragment-Based Screening for the Discovery of Protein-Protein Interaction Stabilizers

Sijbesma, Eline,Hallenbeck, Kenneth K.,Leysen, Seppe,De Vink, Pim J.,Skóra, Lukasz,Jahnke, Wolfgang,Brunsveld, Luc,Arkin, Michelle R.,Ottmann, Christian

supporting information, p. 3524 - 3531 (2019/03/08)

Modulation of protein-protein interactions (PPIs) by small molecules has emerged as a valuable approach in drug discovery. Compared to direct inhibition, PPI stabilization is vastly underexplored but has strong advantages, including the ability to gain se

ipso Nitration in p-halophenyl ethers

Clewley, Robin G.,Fischer, Alfred,Henderson, George N.

, p. 1472 - 1479 (2007/10/02)

Addition of nitronium ion ipso to halogen occurs on nitration of the p-haloanisoles in acetic anhydride at -60 deg C.In the cases of p-fluoro- and p-chloro-anisole, addition of the nitronium ion is reversible and only small amounts of ipso products are obtained.With p-bromoanisole nitrodebromination occurs.When p-halophenyl ethers containing a trapping substituent, e.g., 2-(4-chlorophenoxy)-2-methylpropanoic acid, are used as substrates, substantial amounts of the spiro diene with nitro ipso to halogen, e.g., 3,3-dimethyl-8-chloro-8-nitro-1,4-dioxaspirodeca-6,9-dien-2-one, can be isolated.The results demonstrate that extensive ipso attack at the halogen-substituted position is general in the nitration of p-halophenyl ethers.Key words: ipso nitration, ether, diene, p-haloanisole.

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