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2,7-Dichloro-9H-fluoren-9-one oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22296-44-2

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22296-44-2 Usage

Derivative of fluorenone

A polycyclic aromatic hydrocarbon

Common uses

Reagent in organic synthesis, building block in pharmaceuticals and agrochemicals

Oxime functional group

Useful intermediate in synthesis of nitrogen-containing heterocycles

Dichloro substitution

Unique chemical reactivity in modification and functionalization of organic molecules

Versatile applications

Potential in various areas of chemical research and industry

Check Digit Verification of cas no

The CAS Registry Mumber 22296-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,9 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22296-44:
(7*2)+(6*2)+(5*2)+(4*9)+(3*6)+(2*4)+(1*4)=102
102 % 10 = 2
So 22296-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H7Cl2NO/c14-7-1-3-9-10-4-2-8(15)6-12(10)13(16-17)11(9)5-7/h1-6,17H

22296-44-2SDS

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 N-(2,7-dichlorofluoren-9-ylidene)hydroxylamine

1.2 Other means of identification

Product number -
Other names FLUOREN-9-ONE,2,7-DICHLORO-,OXIME

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:22296-44-2 SDS

22296-44-2Downstream Products

22296-44-2Relevant academic research and scientific papers

Synthesis and structural analysis of halogen substituted fibril formation inhibitors of Human Transthyretin (TTR)

Ciccone, Lidia,Nencetti, Susanna,Rossello, Armando,Stura, Enrico Adriano,Orlandini, Elisabetta

, p. 40 - 51 (2016/12/03)

Transthyretin (TTR), a β-sheet-rich tetrameric protein, in equilibrium with an unstable amyloidogenic monomeric form is responsible for extracellular deposition of amyloid fibrils, is associated with the onset of neurodegenerative diseases, such as senile

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