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895519-91-2

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  • BenzaMide, 4-[(4-Methyl-1-piperazinyl)Methyl]-N-[6-Methyl-5-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-3-pyridinyl]-3-(trifluoroMethyl)-, MonoMethanesulfonate (9CI)

    Cas No: 895519-91-2

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895519-91-2 Usage

Description

BenzaMide, 4-[(4-Methyl-1-piperazinyl)Methyl]-N-[6-Methyl-5-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-3-pyridinyl]-3-(trifluoroMethyl)-, MonoMethanesulfonate (9CI) is a complex organic chemical compound characterized by the presence of a piperazine group, multiple pyridine and pyrimidine rings, a trifluoromethyl group, and a methanesulfonate moiety. BenzaMide, 4-[(4-Methyl-1-piperazinyl)Methyl]-N-[6-Methyl-5-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-3-pyridinyl]-3-(trifluoroMethyl)-, MonoMethanesulfonate (9CI) may hold potential for scientific research and pharmaceutical applications due to its unique structural features and possible biological activity. It is crucial to handle this chemical with appropriate safety measures and precautions.

Uses

Used in Pharmaceutical Research:
BenzaMide, 4-[(4-Methyl-1-piperazinyl)Methyl]-N-[6-Methyl-5-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-3-pyridinyl]-3-(trifluoroMethyl)-, MonoMethanesulfonate (9CI) is used as a research compound for exploring its potential biological activity and therapeutic applications in the pharmaceutical industry. Its unique structure, which includes various heterocyclic rings and functional groups, may contribute to its interaction with biological targets and its potential use in drug development.
Used in Chemical Synthesis:
In the field of chemical synthesis, BenzaMide, 4-[(4-Methyl-1-piperazinyl)Methyl]-N-[6-Methyl-5-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-3-pyridinyl]-3-(trifluoroMethyl)-, MonoMethanesulfonate (9CI) can be utilized as a building block or intermediate in the synthesis of more complex molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Scientific Research:
BenzaMide, 4-[(4-Methyl-1-piperazinyl)Methyl]-N-[6-Methyl-5-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-3-pyridinyl]-3-(trifluoroMethyl)-, MonoMethanesulfonate (9CI) serves as a valuable tool in scientific research, particularly in the study of chemical reactions, mechanisms, and the development of new synthetic methodologies. Its unique structural features and potential reactivity make it an interesting subject for investigation in various research areas.

Check Digit Verification of cas no

The CAS Registry Mumber 895519-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,5,1 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 895519-91:
(8*8)+(7*9)+(6*5)+(5*5)+(4*1)+(3*9)+(2*9)+(1*1)=232
232 % 10 = 2
So 895519-91-2 is a valid CAS Registry Number.

895519-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methanesulfonic acid,4-[(4-methylpiperazin-1-yl)methyl]-N-[6-methyl-5-[(4-pyridin-3-ylpyrimidin-2-yl)amino]pyridin-3-yl]-3-(trifluoromethyl)benzamide

1.2 Other means of identification

Product number -
Other names Flumatinib mesylate

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:895519-91-2 SDS

895519-91-2Downstream Products

895519-91-2Relevant articles and documents

Synthesis, crystal structure, and spectral characterization of flumatinib mesylate

Xu, Gang,Shen, Hong,Tong, Taifeng,Lu, Aifeng,Gou, Shaohua

experimental part, p. 2564 - 2570 (2010/09/30)

Flumatinib mesylate, a 3-substituted picolinamide derivative structurally similar to imatinib mesylate, was prepared. The compound was characterized by infrared, ultraviolet, NMR, and electrospray ionization-mass spectra together with X-ray crystal struct

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