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5-(2-Bromoethyl)hydantoin is an organic compound with the chemical formula C6H8BrNO2. It is a derivative of hydantoin, featuring a bromine atom attached to the ethyl group at the 2-position. 5-(2-Bromoethyl)hydantoin is characterized by its potential reactivity due to the presence of the bromine atom, which can participate in various chemical reactions such as substitution or elimination processes. It is often used in the synthesis of pharmaceuticals and other organic compounds where a bromine-substituted hydantoin structure is required. The compound's properties, such as its reactivity and potential applications, make it a valuable intermediate in organic chemistry and drug development.

7471-52-5

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7471-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7471-52-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7471-52:
(6*7)+(5*4)+(4*7)+(3*1)+(2*5)+(1*2)=105
105 % 10 = 5
So 7471-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H7BrN2O2/c6-2-1-3-4(9)8-5(10)7-3/h3H,1-2H2,(H2,7,8,9,10)

7471-52-5Relevant academic research and scientific papers

Substitution of the phosphonic acid and hydroxamic acid functionalities of the DXR inhibitor FR900098: An attempt to improve the activity against Mycobacterium tuberculosis

Andaloussi, Mounir,Lindh, Martin,Bj?rkelid, Christofer,Suresh, Surisetti,Wieckowska, Anna,Iyer, Harini,Karlén, Anders,Larhed, Mats

scheme or table, p. 5403 - 5407 (2011/10/12)

Two series of FR900098/fosmidomycin analogs were synthesized and evaluated for MtDXR inhibition and Mycobacterium tuberculosis whole-cell activity. The design rationale of these compounds involved the exchange of either the phosphonic acid or the hydroxamic acid part for alternative acidic and metal-coordinating functionalities. The best inhibitors provided IC50 values in the micromolar range, with a best value of 41 μM.

Potential Pancreatic Imaging Agents. Tellurium-123m Labeled DL-α-Amino-γ-(phenyltelluro)butyric Acid

Knapp, Furn F.,Ambrose, Kathleen R.,Callahan, Alvin P.

, p. 794 - 797 (2007/10/02)

This report describes the first successful preparation of a 123mTe-labeled α-amino acid as a potential pancreatic imaging agent.Tellurium-123m labeled DL-α-amino-γ-(phenyltelluro)butyric acid was prepared by basic hydrolysis of the radiolabeled 5-β-(phen

123m Te-Labeled biochemicals and method of preparation

-

, (2008/06/13)

A novel class of 123m Te-labeled steroids and amino acids is provided by the method of reacting a 123m Te symmetric diorgano ditelluride with a hydride reducing agent and a source of alkali metal ions to form an alkali metal organo telluride. The alkali metal organo telluride is reacted with a primary halogenated steroidal side chain, amino acid, or amino acid precursor such as hydantoin. The novel compounds are useful as biological tracers and as organal imaging agents.

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