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1,2-Benzenediamine, 4-fluoro-3-nitrois an aromatic amine chemical compound with a benzene structure, featuring two amino groups and a fluorine and nitro substitution. It is known for its reactivity and is commonly used as an intermediate in the synthesis of various organic compounds, particularly in the production of dyes, pigments, and pharmaceuticals.

147285-79-8

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147285-79-8 Usage

Uses

Used in Dye and Pigment Production:
1,2-Benzenediamine, 4-fluoro-3-nitrois used as a chemical intermediate for the synthesis of dyes and pigments, contributing to the development of a wide range of colorants for various applications.
Used in Pharmaceutical Industry:
1,2-Benzenediamine, 4-fluoro-3-nitrois used as a building block in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medications.
It is important to handle 1,2-Benzenediamine, 4-fluoro-3-nitrowith caution, as it can be hazardous if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 147285-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,8 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147285-79:
(8*1)+(7*4)+(6*7)+(5*2)+(4*8)+(3*5)+(2*7)+(1*9)=158
158 % 10 = 8
So 147285-79-8 is a valid CAS Registry Number.

147285-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-3-nitrobenzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 4-fluoro-3-nitro-benzene-1,2-diamine

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:147285-79-8 SDS

147285-79-8Downstream Products

147285-79-8Relevant academic research and scientific papers

An improved procedure for the nitration of benzo-2,1,3-selenadiazoles and their reduction to ortho-phenylenediamines

Wright,McClure

, p. 1023 - 1026 (2007/10/03)

A method for the nitration of benzo-2,1,3-selenadiazoles using nitric acid dissolved in a mixture of methanesulfonic acid and phosphorus pentoxide at room temperature is presented. The SN2Ar displacement of fluoride that is observed when sulfur

Nitration of 5-Fluoro-2,1,3-benzoselenadiazoles, and the Synthesis of 4-Fluoro-3-nitro-, 4-Fluoro-6-nitro, 5-Fluoro-3-nitro-o-phenylenediamines and 3,4-Diamino-2-nitrophenols by Subsequent Deselenation

Tian, Wei,Grivas, Spiros,Olsson, Kjell

, p. 257 - 262 (2007/10/02)

Fuming nitric and concentrated sulfuric acids converted the title benzoselenadiazoles 1 and 8 into their 4- and/or 7-nitro derivatives.Unlike the m-fluoronitro substituted products 6 and 9, the o-fluoronitro substituted products 2 were accompanied by the

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