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2-(2-aMino-5-fluorophenyl)acetohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

356068-89-8

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356068-89-8 Usage

Molecular weight

182.19 g/mol

Chemical class

Hydrazide derivative

Structure

An acetohydrazide moiety with a substituted fluorophenyl ring

Usage

Building block in organic synthesis and pharmaceutical research for the preparation of biologically active compounds

Value in drug discovery

Unique structure and properties make it a valuable tool in the development of new drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 356068-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,0,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 356068-89:
(8*3)+(7*5)+(6*6)+(5*0)+(4*6)+(3*8)+(2*8)+(1*9)=168
168 % 10 = 8
So 356068-89-8 is a valid CAS Registry Number.

356068-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-5-fluoro-phenyl)-acetic acid hydrazide

1.2 Other means of identification

Product number -
Other names (2-amino-5-fluoro-phenyl)acetic acid hydrazide

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:356068-89-8 SDS

356068-89-8Upstream product

356068-89-8Downstream Products

356068-89-8Relevant academic research and scientific papers

Treatment of excessive osteolysis with indolinone compounds

-

, (2008/06/13)

Compounds of Formula I and Formula II, as described herein, are useful for treating excessive osteolysis, by inhibiting M-CSF mediated osteoclast development. The compounds also are useful for inhibiting phosphorylation of CSF1R, and for treating cancers that express CSF1R.

Hexahydro-cyclohepta-pyrrole oxindole as potent kinase inhibitors

-

Page/Page column 20, (2010/02/08)

The present invention is directed to a class indolinone compounds, hexahydro-cyclohepta-pyrrole oxindoles, which are useful as protein kinase inhibitors.

Combination therapy for the treatment of cancer

-

, (2008/06/13)

The present invention relates to methods for treatment or prevention of neoplasia disorders using protein tyrosine kinase inhibitors in combination with cyclooxygenase inhibitors, in particular cyclooxygenase-2 selective inhibitors.

Treatment of acute myeloid leukemia with indolinone compounds

-

, (2008/06/13)

A method of treating acute myeloid leukemia in patient positive for FLT-3-ITD is described. The treatment is accomplished by administration of a compound of Formula I or II as defined herein.

Prodrugs of a 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives

-

, (2008/06/13)

The present invention relates to pyrrole substituted 2-indolinone compounds and their pharmaceutically acceptable salts which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.

Mannich base prodrugs of 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives

-

, (2008/06/13)

The present invention is directed to Mannich base prodrugs of certain 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives that modulate the activity of protein kinases (“PKs”). Pharmaceutical compositions comprising these compounds, methods of treating diseases related to abnormal PK activity utilizing pharmaceutical compositions comprising these compounds and methods of preparing them are also disclosed.

Pyrrole substituted 2-indolinone protein kinase inhibitors

-

, (2008/06/13)

The present invention relates to pyrrole substituted 2-indolinone compounds and their pharmaceutically acceptable salts which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.

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