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"N-butyl-N-{[1-(2-methylbenzyl)-1H-pyrrol-2-yl]methyl}-2-phenylcyclopropanecarboxamide" is a complex organic compound with a molecular formula of C27H30N2O. It is a derivative of cyclopropanecarboxamide, featuring a butyl group, a phenyl group, and a pyrrole ring with a methylbenzyl substituent. N-butyl-N-{[1-(2-methylbenzyl)-1H-pyrrol-2-yl]methyl}-2-phenylcyclopropanecarboxamide is characterized by its unique structure, which includes a cyclopropane ring, a pyrrole ring, and an amide linkage. It is synthesized through a series of chemical reactions and is typically used in the field of pharmaceuticals and organic chemistry for its potential therapeutic applications and as a building block for more complex molecules. The compound's specific properties and reactivity are determined by its molecular structure, making it a subject of interest for researchers in drug development and chemical synthesis.

5937-86-0

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5937-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5937-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5937-86:
(6*5)+(5*9)+(4*3)+(3*7)+(2*8)+(1*6)=130
130 % 10 = 0
So 5937-86-0 is a valid CAS Registry Number.

5937-86-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-N-[[1-[(2-methylphenyl)methyl]pyrrol-2-yl]methyl]-2-phenylcyclopropane-1-carboxamide

1.2 Other means of identification

Product number -
Other names -

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5937-86-0 SDS

5937-86-0Downstream Products

5937-86-0Relevant academic research and scientific papers

Synthesis of a series of novel dihydroartemisinin derivatives containing a substituted chalcone with greater cytotoxic effects in leukemia cells

Yang, Xuelin,Wang, Wei,Tan, Jun,Song, Dandan,Li, Ming,Liu, Dan,Jing, Yongkui,Zhao, Linxiang

experimental part, p. 4385 - 4388 (2010/04/05)

Fifteen dihydroartemisinin derivatives containing a substituted chalcone linked by either ether or ester were synthesized and investigated for their cytotoxicity in human leukemia HL-60 and mouse lymphoma P388 cells. These derivatives have greater antiproliferative and cytotoxic effects in both cell lines than dihydroartemisinin. Dihydroartemisinin chalcones linked by ether are more cytotoxic than dihydroartemisinin chalcones linked by ester with apoptosis induction abilities.

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