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5-hydroxy-2-(1-propyl)isoindole-1,3-dione is a chemical compound with the molecular formula C12H11NO3. It is a derivative of isoindole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a pyrrolidine ring. The compound features a hydroxyl group (-OH) at the 5-position, a propyl group (-CH2CH2CH3) at the 2-position, and two carbonyl groups (C=O) at the 1 and 3 positions. This specific arrangement of functional groups gives the molecule unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. However, further research and characterization are needed to fully understand its potential uses and properties.

3913-46-0

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3913-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3913-46-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3913-46:
(6*3)+(5*9)+(4*1)+(3*3)+(2*4)+(1*6)=90
90 % 10 = 0
So 3913-46-0 is a valid CAS Registry Number.

3913-46-0Relevant academic research and scientific papers

Design and synthesis of an orally active metabotropic glutamate receptor subtype-2 (mGluR2) positive allosteric modulator (PAM) that decreases cocaine self-administration in rats

Dhanya, Raveendra-Panickar,Sidique, Shyama,Sheffler, Douglas J.,Nickols, Hilary Highfield,Herath, Ananda,Yang, Li,Dahl, Russell,Ardecky, Robert,Semenova, Svetlana,Markou, Athina,Conn, P. Jeffrey,Cosford, Nicholas D. P.

experimental part, p. 342 - 353 (2011/03/18)

The modification of 3′-((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3- dihydro-1H-inden-5-yloxy)methyl)biphenyl-4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties. These analogues are more potent than 1 in vitro and are highly selective for mGluR2 vs other mGluR subtypes. They have significantly improved pharmacokinetic (PK) properties, with excellent oral bioavailability and brain penetration. The benzisothiazol-3-one derivative 14 decreased cocaine self-administration in rats, providing proof-of-concept for the use of mGluR2 PAMs for the treatment of cocaine dependence.

Development of tryptase inhibitors derived from thalidomide

Tetsuhashi, Masashi,Ishikawa, Minoru,Hashimoto, Mariko,Hashimoto, Yuichi,Aoyama, Hiroshi

experimental part, p. 5323 - 5338 (2010/09/15)

A novel series of tryptase inhibitors with a N-phenylphthalimide skeleton structurally derived from thalidomide (1) has been developed. Structure-activity relationship studies led to a potent and selective tryptase inhibitor, 2-(4-cyanophenyl)isoindole-1,3-dione-5-yl 3-(2-aminopyridin-5-yl)propanoate (7), with the IC50 value of 78 nM.

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