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Cyclopropyl(4-(dimethylamino)phenyl)methanone is a chemical compound with the molecular formula C13H15NO. It belongs to the class of ketones and is commonly used in organic synthesis and pharmaceutical research. cyclopropyl(4-(dimethylamino)phenyl)methanone consists of a cyclopropyl group attached to a phenyl ring substituted with a dimethylamino group and a carbonyl group. Its unique structure and reactivity make it a versatile building block for the synthesis of various pharmaceuticals and agrochemicals. Additionally, cyclopropyl(4-(dimethylamino)phenyl)methanone has been studied for its potential use in the treatment of neurological disorders and as a component in the design of new drug molecules with improved biological activity.

7450-85-3

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7450-85-3 Usage

Uses

Used in Pharmaceutical Research:
Cyclopropyl(4-(dimethylamino)phenyl)methanone is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and reactivity. It aids in the development of new drug molecules with improved biological activity.
Used in Agrochemical Synthesis:
In the agrochemical industry, cyclopropyl(4-(dimethylamino)phenyl)methanone is used as a key intermediate in the synthesis of various agrochemicals, contributing to the development of effective pest control solutions.
Used in Neurological Disorder Treatment:
Cyclopropyl(4-(dimethylamino)phenyl)methanone is studied for its potential use in the treatment of neurological disorders, as it may contribute to the development of novel therapeutic agents targeting these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 7450-85-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,5 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7450-85:
(6*7)+(5*4)+(4*5)+(3*0)+(2*8)+(1*5)=103
103 % 10 = 3
So 7450-85-3 is a valid CAS Registry Number.

7450-85-3Downstream Products

7450-85-3Relevant academic research and scientific papers

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

Pandey, Ganesh,Tiwari, Sandip Kumar,Singh, Bhawana,Vanka, Kumar,Jain, Shailja

supporting information, p. 12337 - 12340 (2017/11/20)

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.

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