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3,4-di(4-morpholinyl)-4-phenyl-2-butanone is a complex organic compound with the molecular formula C20H27NO4. It is a derivative of 2-butanone, featuring two morpholinyl groups attached to the 3rd and 4th carbon atoms, and a phenyl group on the 4th carbon. 3,4-di(4-morpholinyl)-4-phenyl-2-butanone is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. Its structure provides a unique combination of functional groups, which can be exploited for the development of new therapeutic agents. The compound's properties, such as solubility and reactivity, are influenced by the presence of the morpholinyl and phenyl groups, making it a versatile building block in organic synthesis.

5455-91-4

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5455-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5455-91-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5455-91:
(6*5)+(5*4)+(4*5)+(3*5)+(2*9)+(1*1)=104
104 % 10 = 4
So 5455-91-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H26N2O3/c1-15(21)17(19-7-11-22-12-8-19)18(16-5-3-2-4-6-16)20-9-13-23-14-10-20/h2-6,17-18H,7-14H2,1H3

5455-91-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimorpholin-4-yl-4-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 3,4-dimorpholino-4-phenyl-butan-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:5455-91-4 SDS

5455-91-4Relevant academic research and scientific papers

Iodine-promoted Intermolecular Dehydrogenation Diamination: Synthesis of Unsymmetrical α,β-Diamido Ketones

Zhang, YongJian,Su, Junyi,Niu, Wenjie,Li, Yujin

supporting information, p. 1477 - 1480 (2019/03/26)

Iodine-promoted direct diamination of α,β-unsaturated ketone to form two C?N bonds has been developed starting from chalcone and secondary amine. This reaction was performed in THF at 50 °C in the presence of I2 and K2CO3.

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