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1069085-50-2

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1069085-50-2 Usage

General Description

2-(DifluoroMethyl)-1-phenyl-4,5-dihydro-1H-iMidazole, also known as Fimasertib, is a chemical compound with the molecular formula C10H10F2N2. It belongs to the class of imidazole derivatives and is used in the pharmaceutical industry as a kinase inhibitor for the treatment of various diseases. Fimasertib has shown potential for the treatment of cancer, particularly in combination with other drugs. It works by inhibiting the activities of specific kinases, thereby preventing the growth and spread of cancer cells. Fimasertib is currently under investigation in clinical trials for the treatment of various types of cancers, making it a promising candidate for the development of new cancer therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 1069085-50-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,9,0,8 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1069085-50:
(9*1)+(8*0)+(7*6)+(6*9)+(5*0)+(4*8)+(3*5)+(2*5)+(1*0)=162
162 % 10 = 2
So 1069085-50-2 is a valid CAS Registry Number.

1069085-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(difluoromethyl)-1-phenyl-4,5-dihydroimidazole

1.2 Other means of identification

Product number -
Other names 1-phenyl-2-difluoromethylimidazoline

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:1069085-50-2 SDS

1069085-50-2Downstream Products

1069085-50-2Relevant articles and documents

A facile one-pot synthesis of 2-fluoroalkyl 1,3-imidazolines and 1,3-oxazolines through imidoyl halide intermediates

Jiang, Haizhen,Sun, Lan,Yuan, Shijie,Lu, Wenjun,Wan, Wen,Zhu, Shizheng,Hao, Jian

supporting information; experimental part, p. 2858 - 2863 (2012/05/05)

A facile one-pot procedure has been developed for the synthesis of 1,3-imidazolines and 1,3-oxazolines bearing fluorinated alkyl groups at the 2-position. The reaction involves the condensation of N-monosubstituted ethane-1,2-diamines or 2-aminoethanols with a fluorinated carboxylic acid in the presence of PPh3/CX4. The proposed mechanism is that the amide intermediates were initially formed, and then converted to the imidoyl halide intermediates in the presence of PPh3/CX4, followed by rapid intramolecular cyclization to 1,3-diazoline products. This protocol allows for the synthesis of 2-bromodifluoromethyl-1,3-imidazoline, a useful CF2Br-heterocyclic building block, which can be used for the synthesis of gem-difluoromethylene linked compounds.

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