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2-FLUORO-5-NITROPHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22510-08-3

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22510-08-3 Usage

Uses

2-Fluoro-5-nitrophenol

Check Digit Verification of cas no

The CAS Registry Mumber 22510-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,1 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22510-08:
(7*2)+(6*2)+(5*5)+(4*1)+(3*0)+(2*0)+(1*8)=63
63 % 10 = 3
So 22510-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H4FNO3/c7-5-2-1-4(8(10)11)3-6(5)9/h1-3,9H

22510-08-3SDS

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 2-Fluoro-5-nitrophenol

1.2 Other means of identification

Product number -
Other names 2-Fluoro-5-Nitrophenol

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:22510-08-3 SDS

22510-08-3Relevant academic research and scientific papers

CINNOLINE COMPOUNDS AS INHIBITORS OF PHOSPHODIESTERASE TYPE IV (PDE4)

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Page/Page column 65-66, (2010/11/27)

There are provided according to the invention novel compounds of formula (I).

Rates of reductive elimination of substituted nitrophenols from the (indol-3-yl)methyl position of indolequinones

Swann,Moody,Stratford,Patel,Naylor,Vojnovic,Wardman,Everett

, p. 1340 - 1345 (2007/10/03)

A series of indolequinones bearing substituted nitrophenols on the (indol-3-yl)methyl position was synthesised. The nitrophenol leaving groups were appropriately substituted to give a wide range (4 units) in phenolic pKa value. The rate of redu

1-[4-(4'-sulfanilyl)phenyl]urea and derivatives for the treatment of Leishmaniasis

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, (2008/06/13)

1-[4-(4'-sulfanilyl)phenyl]urea and its various substituted derivatives can be used to decrease the infectiousness of and reduce the mortality associated with organisms of the genus Leishmania which are responsible for a group of conditions known as Leish

Phenyl benzoic acid compounds

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, (2008/06/13)

The invention relates to substituted 5-(phenyl)benzoic acid esters and non-toxic pharmaceutically accepted salts thereof and processes for their preparation. The substituted 5-(phenyl)benozic acids are useful as anti-inflammatory compounds. Also included are method of treating inflammation claims by administering these particular compounds to patients.

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