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α-Fluoro-γ-butyrolactone is a chemical compound with the molecular formula C4H5FO2. It is a cyclic ester derived from γ-butyrolactone, featuring a fluorine atom at the α-position. This fluorinated lactone is an important building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Due to the presence of fluorine, it can significantly alter the physical and chemical properties of the molecules in which it is incorporated, such as enhancing lipophilicity and metabolic stability. α-Fluoro-γ-butyrolactone is synthesized through various methods, including the reaction of γ-butyrolactone with fluorinating agents, and it is known for its reactivity in various chemical transformations, making it a valuable intermediate in the synthesis of fluorinated organic compounds.

3885-31-2

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3885-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3885-31-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3885-31:
(6*3)+(5*8)+(4*8)+(3*5)+(2*3)+(1*1)=112
112 % 10 = 2
So 3885-31-2 is a valid CAS Registry Number.

3885-31-2Upstream product

3885-31-2Downstream Products

3885-31-2Relevant academic research and scientific papers

IRAK4 INHIBITING AGENTS

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Page/Page column 282, (2016/03/13)

Provided are compounds of Formula (I), or pharmaceutically acceptable salts thereof, and methods for their use and production.

Development of Fluorine-18 Labeled Metabolically Activated Tracers for Imaging of Drug Efflux Transporters with Positron Emission Tomography

Sander, Kerstin,Galante, Eva,Gendron, Thibault,Yiannaki, Elena,Patel, Niral,Kalber, Tammy L.,Badar, Adam,Robson, Mathew,Johnson, Sean P.,Bauer, Florian,Mairinger, Severin,Stanek, Johann,Wanek, Thomas,Kuntner, Claudia,Kottke, Tim,Weizel, Lilia,Dickens, David,Erlandsson, Kjell,Hutton, Brian F.,Lythgoe, Mark F.,Stark, Holger,Langer, Oliver,Koepp, Matthias,?rstad, Erik

, p. 6058 - 6080 (2015/08/24)

Increased activity of efflux transporters, e.g., P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), at the blood-brain barrier is a pathological hallmark of many neurological diseases, and the resulting multiple drug resistance represents a major clinical challenge. Noninvasive imaging of transporter activity can help to clarify the underlying mechanisms of drug resistance and facilitate diagnosis, patient stratification, and treatment monitoring. We have developed a metabolically activated radiotracer for functional imaging of P-gp/BCRP activity with positron emission tomography (PET). In preclinical studies, the tracer showed excellent initial brain uptake and clean conversion to the desired metabolite, although at a sluggish rate. Blocking with P-gp/BCRP modulators led to increased levels of brain radioactivity; however, dynamic PET did not show differential clearance rates between treatment and control groups. Our results provide proof-of-concept for development of prodrug tracers for imaging of P-gp/BCRP function in vivo but also highlight some challenges associated with this strategy.

Syntheses of fluorinated ligands to probe binding of antigenic determinants of Vibrio cholerae O:1, serotypes Inaba and Ogawa, to antibodies

Chang, Alex H.C.,Horton, Derek,Kovac, Pavol

, p. 595 - 606 (2007/10/03)

Derivatives of methyl α-glycosides of antigenic determinants of Vibrio cholerae O:1, serotypes Inaba and Ogawa, specifically fluorinated at position 2' or 4' have been synthesized by coupling the appropriately fluorinated derivatives of 3-deoxy-L-glycero-tetronic acid with the methyl α-glycosides of perosamine. The compound having the fluorine atom at position 2 was obtained by electrophilic addition of fluorine to the glycal derived from the parent antigenic determinant, serotypes Inaba, using Selectfluor((TM)) as a fluorination reagent. Copyright (C) 2000 Elsevier Science Ltd.

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