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2105-96-6

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2105-96-6 Usage

General Description

4-Fluoro-3-nitrophenol is a type of aromatic compound that belongs to the family of nitrophenols, which are phenols carrying one or more nitro functional groups. The '4-Fluoro-3-nitrophenol' features a nitro group in the 3rd position on the benzene ring and a fluorine atom in the 4th position. 4-Fluoro-3-nitrophenol is typically a yellow solid and possesses the molecular formula C6H4FNO3. Its chemical properties like solubility, melting point, and boiling point vary according to different conditions. It's mainly used in the field of pharmaceuticals, materials science, and organic synthesis. Like other nitrophenols, 4-Fluoro-3-nitrophenol should be handled carefully as it may pose health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 2105-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2105-96:
(6*2)+(5*1)+(4*0)+(3*5)+(2*9)+(1*6)=56
56 % 10 = 6
So 2105-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H4FNO3/c7-5-2-1-4(9)3-6(5)8(10)11/h1-3,9H

2105-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-3-nitrophenol

1.2 Other means of identification

Product number -
Other names Phenol,4-fluoro-3-nitro

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:2105-96-6 SDS

2105-96-6Relevant articles and documents

Fluorinated xanthene derivatives

-

, (2008/06/13)

The family of dyes of the invention are fluoresceins and rhodols that are directly substituted on one or more aromatic carbons by fluorine. These fluorine-substituted fluorescent dyes possess greater photostability and have lower sensitivity to pH changes in the physiological range of 6-8 than do non-fluorinated dyes, exhibit less quenching when conjugated to a substance, and possess additional advantages. The dyes of the invention are useful as detectable tracers and for preparing conjugates of organic and inorganic substances.

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