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1-Propanone, 1-(2-amino-5-chlorophenyl)-3-phenyl- is a complex organic compound with the chemical formula C15H14ClNO. It is a derivative of propanone, featuring a 2-amino-5-chlorophenyl group attached to the first carbon and a phenyl group attached to the third carbon. 1-Propanone, 1-(2-amino-5-chlorophenyl)-3-phenyl- is characterized by its unique structure, which includes a ketone functional group, an amine group, and a chlorine atom. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile reactivity and the presence of multiple functional groups. The compound's properties, such as its solubility and stability, can be influenced by the presence of the chlorine atom and the amino group, making it a valuable building block in organic synthesis.

1971-18-2

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1971-18-2 Usage

Chemical classification

1-Propanone, 1-(2-amino-5-chlorophenyl)-3-phenylis a ketone, which is a type of organic compound with a carbonyl group (C=O) bonded to two alkyl or aryl groups.

Molecular weight

261.7 g/mol, which is the mass of one mole of the compound.

Aromatic and phenyl properties

The compound contains a phenyl group (a ring of six carbon atoms with alternating single and double bonds), and is known for its aromatic properties, meaning it has a stable, delocalized electron system.

Check Digit Verification of cas no

The CAS Registry Mumber 1971-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1971-18:
(6*1)+(5*9)+(4*7)+(3*1)+(2*1)+(1*8)=92
92 % 10 = 2
So 1971-18-2 is a valid CAS Registry Number.

1971-18-2Downstream Products

1971-18-2Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF TUMORS

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Page/Page column 252-253, (2021/06/22)

The present invention relates to compounds of Formula (Ia) or pharmaceutically acceptable salts, hydrates, solvates, clathrates, polymorphs, stereoisomers thereof. It further discloses a pharmaceutical composition comprising compounds of Formula (Ia) and the use of compounds of Formula (Ib), in particular for the use in the treatment of diseases or disorders wherein disrupting Rad51-BRCA2 interaction is beneficial.

Convenient synthetic approach to 2,4-disubstituted quinazolines

Ferrini, Serena,Ponticelli, Fabio,Taddei, Maurizio

, p. 69 - 72 (2007/10/03)

(Chemical Equation Presented) 2,4-Dialkyl or aryl quinazolines have been prepared in three steps starting from easily available anilides. A photochemically induced Fries rearrangement of the anilides gave several ortho-aminoacylbenzene derivatives that we

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