Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1160294-26-7

Post Buying Request

1160294-26-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • high quality (Z)-methyl 3-((4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)phenylamino)(phenyl)methylene)-2-oxoindoline-6-carboxylate

    Cas No: 1160294-26-7

  • USD $ 1.0-1.0 / Kilogram

  • 1 Kilogram

  • 10 Gram/Day

  • Henan Tianfu Chemical Co., Ltd.
  • Contact Supplier
  • 1H-Indole-6-carboxylic acid, 2,3-dihydro-3-[[[4-[methyl[2-(4-methyl-1-piperazinyl)acetyl]amino]phenyl]amino]phenylmethylene]-2-oxo-, methyl ester

    Cas No: 1160294-26-7

  • No Data

  • No Data

  • No Data

  • Antimex Chemical Limied
  • Contact Supplier
  • Methyl (3Z)-3-{[(4-{methyl[(4-methyl-1-piperazinyl)acetyl]amino}p henyl)amino](phenyl)methylene}-2-oxo-6-indolinecarboxylate

    Cas No: 1160294-26-7

  • No Data

  • No Data

  • No Data

  • Chemlyte Solutions
  • Contact Supplier

1160294-26-7 Usage

General Description

(Z)-methyl 3-((4-(N-methyl-2-(4-methylpiperazin-1-yl)acetamido)phenylamino)(phenyl)methylene)-2-oxoindoline-6-carboxylate is a complex chemical compound with a lengthy and intricate molecular structure. It contains various functional groups including ester, amide, and amine functionalities, and it is characterized by its indoline and phenyl rings. This chemical is of interest due to its potential pharmaceutical applications, particularly in the field of drug development. Its precise properties and potential uses would need to be further investigated through extensive study and analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 1160294-26-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,2,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1160294-26:
(9*1)+(8*1)+(7*6)+(6*0)+(5*2)+(4*9)+(3*4)+(2*2)+(1*6)=127
127 % 10 = 7
So 1160294-26-7 is a valid CAS Registry Number.

1160294-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (3Z)-3-{[(4-{methyl[(4-methyl-1-piperazinyl)acetyl]amino}p henyl)amino](phenyl)methylene}-2-oxo-6-indolinecarboxylate

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:1160294-26-7 SDS

1160294-26-7Downstream Products

1160294-26-7Relevant articles and documents

Synthesis of the Kinase Inhibitors Nintedanib, Hesperadin, and Their Analogues Using the Eschenmoser Coupling Reaction

Marek, Luká?,Váňa, Ji?í,Svoboda, Jan,Hanusek, Ji?í

, p. 10621 - 10629 (2021/07/31)

A novel synthetic approach involving an Eschenmoser coupling reaction of substituted 3-bromooxindoles (H, 6-Cl, 6-COOMe, 5-NO2) with two substituted thiobenzanilides in dimethylformamide or acetonitrile was used for the synthesis of eight kinase inhibitor

METHODS FOR PREPARING NINTEDANIB AND INTERMEDIATES THEREOF

-

Sheet 0069, (2020/02/27)

The present application provides a method for preparing nintedanib. The method of the present application is carried out by using 4-halo-3-nitro-benzoic acid methyl ester (compound II) and 3-oxo-3-phenylpropionate (compound III) as raw materials, and prep

Preparation method of nintedanib key intermediate

-

Paragraph 0069-0074, (2020/10/27)

The invention belongs to the technical field of pharmaceutical chemicals, and particularly relates to a preparation method of a nintedanib key intermediate compound II. A compound IV is reduced by adopting a common reaction reagent under the conditions of normal temperature and normal pressure, so that a high-purity compound II can be conveniently obtained. The adopted reaction conditions are mild, high-pressure equipment is avoided, the technical operation is simple, the conditions are mild, the process is safer and more environmentally friendly, and the feasibility of large-scale productionof nintedanib is greatly improved.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1160294-26-7