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1-[Bis-(4-fluoro-phenyl)-methyl]-azetidin-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116574-15-3

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116574-15-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Azetidines are a class of organic compounds that contain a four-membered ring with three carbon atoms and one nitrogen atom.

Explanation

The compound is a solid at room temperature and appears white in color.

Explanation

The compound is frequently utilized in research and development processes, likely due to its unique structure and potential pharmacological activities.

Explanation

The compound has been investigated for its possible applications in medicine, particularly in the development of new drugs.

Explanation

The compound's structure features a bis-(4-fluoro-phenyl)-methyl group connected to an azetidin-3-ol ring, which may contribute to its diverse range of potential applications.

Explanation

While the compound has shown promise in certain areas, more research is required to comprehensively understand its properties, potential benefits, and possible applications.

Class

Azetidines

Physical state

White solid

Research and development

Commonly used

Potential pharmacological activities

Studied in the field of medicinal chemistry

Unique structure

Bis-(4-fluoro-phenyl)-methyl group attached to an azetidin-3-ol ring

Further research needed

To fully understand properties and uses

Check Digit Verification of cas no

The CAS Registry Mumber 116574-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,7 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116574-15:
(8*1)+(7*1)+(6*6)+(5*5)+(4*7)+(3*4)+(2*1)+(1*5)=123
123 % 10 = 3
So 116574-15-3 is a valid CAS Registry Number.

116574-15-3Relevant academic research and scientific papers

Novel 2-amino-1,4-dihydropyridine calcium antagonists. II. Synthesis and antihypertensive effects of 2-amino-1,4-dihydropyridine derivatives having N,N-dialkylaminoalkoxycarbonyl groups at 3- and/or 5-positions

Kobayashi,Inoue,Nishino,Fujihara,Oizumi,Kimura

, p. 797 - 817 (1995)

Novel 2-amino-1,4-dihydropyridine derivatives I, which contain N,N-dialkylaminoalkoxycarbonyl groups at the 3- and/or 5-position, were synthesized and their antihypertensive effects were evaluated in spontaneously hypertensive rats. Remarkably prolonged duration of antihypertensive action was observed when a tertiary amino group was introduced into either the 3- or 5-ester side-chain of the 1,4-dihydropyridine ring. In particular, the compounds containing cyclic amino moieties at the 3-position showed greater potency than those with acyclic amino moieties. Chemical modification studies indicated that the two ester side-chains of 1,4-dihydropyridine at the 3- and 5-position might function in a different manner in relation to the antihypertensive activities. 3-(1-Benzhydrylazetidin-3-yl) 5-isopropyl 2-amino-1,4-dihydro-6-methyl-4-(3-nitrophenyl)-3,5-pyridine-dicarboxyl ate, I-43 (CS-905), exhibited potent and long-lasting antihypertensive effects with gradual onset of action, and is a promising candidate as an antihypertensive drug.

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