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1-Propanone, 3-[(4-chlorophenyl)amino]-1-(4-nitrophenyl)-3-phenyl- is a complex organic compound with the molecular formula C20H17ClN2O3. It is a derivative of propanone, featuring a 4-chlorophenyl group attached to the amino group, a 4-nitrophenyl group at the 1-position, and a phenyl group at the 3-position. 1-Propanone, 3-[(4-chlorophenyl)amino]-1-(4-nitrophenyl)-3-phenyl- is characterized by its unique structure, which combines the properties of a ketone, an amine, and an aromatic system. It is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its diverse functional groups, which can participate in various chemical reactions. The presence of a chlorine atom and a nitro group also suggests potential applications in the development of agrochemicals or as intermediates in the synthesis of other complex molecules.

4210-10-0

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4210-10-0 Usage

Type of compound

ketone

Substituents

+ Substituted phenyl group
+ 4-chlorophenylamino group
+ 4-nitrophenyl group attached to the 3-position of the ketone

Contains 3 phenyl rings

one in the 1-Propanone part and two in the substituent groups

Contains 3 nitrogen atoms

one in the 4-chlorophenylamino group and two in the 1-(4-nitrophenyl)-3-phenylpart

Contains 3 oxygen atoms

one in the 1-Propanone part and two in the 1-(4-nitrophenyl)-3-phenylpart

Potential applications

pharmaceuticals, organic synthesis, development of new drugs, building block for more complex molecules
Requires further research and testing to understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 4210-10-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4210-10:
(6*4)+(5*2)+(4*1)+(3*0)+(2*1)+(1*0)=40
40 % 10 = 0
So 4210-10-0 is a valid CAS Registry Number.

4210-10-0Downstream Products

4210-10-0Relevant academic research and scientific papers

K3PO4-catalyzed one-pot synthesis of β-amino ketones

Movassagh, Barahman,Khosousi, Sakineh

, p. 1503 - 1506 (2013/02/21)

A new strategy which uses cheap K3PO4 as a very effective catalyst has been developed for synthesis of β-amino ketones by one-pot reaction of an aryl aldehyde, acetophenone derivative, and amine in EtOH at room temperature. Springer-Verlag 2012.

SnCl45H2O-catalyzed synthesis of β-amino carbonyl compounds via a direct Mannich-type reaction

Wang, Min,Song, Zhiguo,Liang, Yan

experimental part, p. 1 - 6 (2011/12/22)

An efficient three-component, one-pot synthesis of β-amino carbonyl compounds from aromatic ketones, aromatic aldehydes, and aromatic amines using tin tetrachloride at room temperature in ethanol is described. The advantages of the new method are good yields (62-96%), simple workup, and inexpensive catalyst. Copyright Taylor & Francis Group, LLC.

Aluminium nitrate as an efficient and reusable catalyst for the three components one-pot Mannich reaction: Synthesis of β-amino carbonyl compounds

Wang, Min,Liang, Yan,Song, Zhiguo

supporting information; experimental part, p. 1653 - 1656 (2011/02/21)

Three components one-pot Mannich reaction of aromatic ketones, aromatic aldehydes and aromatic amines has been efficiently catalysed by recyclable aluminium nitrate at ambient temperature to give various β-amino carbonyl compounds in high yields. By simple phase separation, aluminium nitrate could be recycled several times without distinct loss of activity.

Non-Steroidal Androgen Receptor Modulators, Preparation Process, Pharmaceutical Composition and Use Thereof

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Page/Page column 7, (2009/01/20)

Non-steroidal androgen receptor modulating compounds of the general formula (I), their pharmaceutically acceptable salts, preparation process and pharmaceutically compositions containing the said compounds are disclosed. Such compounds of the general formula (I) or their pharmaceutically acceptable salts can be used for preparing non-steroidal medicines to treat and/or prevent conditions or diseases such as prostatic hyperplasia, prostate cancer, hirsutism, severe hormone-dependent alopecia or acne, etc. as a result of androgen receptor antagonistic activities.

NONSTEROIC ANDROGEN ACCEPTOR REGULATORS, PREPARATION PROCESS, PHARMACEUTICAL COMPOSITION AND USE THEREOF

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Page/Page column 11, (2010/11/30)

Nons-teroidal androgen receptor modulating compounds of the general formula (I), their pharmaceutically acceptable salts, preparation process and pharmaceutically compositions containing the said compounds are disclosed. Such compounds of the general formula (I) or their pharmaceutically acceptable salts can be used for preparing non-steroidal medicines to treat and/or prevent condictions or diseases such as prostatic hyperplasia, prostate cancer, hirsutism, severe hormone-dependent alopecia or acne, etc. as a result of androgen receptor antagonistic activities.

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