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2-Azetidinone, 3-methyl-3-phenyl-1-(phenylmethyl)-, also known as 3-Methyl-3-phenyl-1-benzyl-2-azetidinone, is a chemical compound with the molecular formula C16H15NO. It is a derivative of azetidinone, a four-membered cyclic amide, and features a methyl group at the 3-position, a phenyl group at the 3-position, and a benzyl group at the 1-position. 2-Azetidinone, 3-methyl-3-phenyl-1-(phenylmethyl)- is primarily used in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is an important intermediate in the development of drugs targeting the central nervous system and other therapeutic applications.

2025-77-6

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2025-77-6 Usage

Type

Cyclic amide

Common uses

Organic synthesis, pharmaceutical research

Potential applications

Development of pharmaceutical drugs and bioactive molecules

Value

Valuable ingredient in the synthesis of organic compounds with medical and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 2025-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,2 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2025-77:
(6*2)+(5*0)+(4*2)+(3*5)+(2*7)+(1*7)=56
56 % 10 = 6
So 2025-77-6 is a valid CAS Registry Number.

2025-77-6Downstream Products

2025-77-6Relevant academic research and scientific papers

Solid-phase synthesis of monocyclic β-lactam derivatives

Schunk,Enders

, p. 8034 - 8042 (2007/10/03)

Liquid-phase studies concerning the solid-phase synthesis of monocyclic β-lactams via the esterenolate imine condensation route have been conducted utilizing triazene esters 1 and 2 as model compounds. Esters were attached to benzylamine resin 6 by a triazene linker employing the respective diazonium salts. Immobilized ester-enolates 8 and 10 were reacted with various imines and imine precursors to give polymer-bound β-lactams 14 and 17 in different substitution patterns. Traceless cleavage from the triazene linker yields the desired β-lactams 16 and 19.

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