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2-CHLORO-4-NITRO-N-METHYLANILINE, also known as 4-nitro-2-chloro-N-methylaniline, is a chemical compound characterized by the molecular formula C7H7ClN2O2. It presents as a yellow solid that is insoluble in water but readily soluble in organic solvents. 2-CHLORO-4-NITRO-N-METHYLANILINE is utilized as a crucial intermediate in the synthesis of dyes, pigments, pharmaceuticals, and agrochemicals, highlighting its importance in various industrial applications. However, it is also recognized as a potential environmental contaminant with toxic effects on aquatic life, necessitating careful handling and storage to mitigate health and environmental risks.

6085-92-3

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6085-92-3 Usage

Uses

Used in Chemical Synthesis Industry:
2-CHLORO-4-NITRO-N-METHYLANILINE is used as a chemical intermediate for the production of various dyes and pigments, contributing to the coloration and appearance of a wide range of products. Its role in this industry is vital for creating the vibrant colors seen in textiles, plastics, and other materials.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-CHLORO-4-NITRO-N-METHYLANILINE serves as a key intermediate in the synthesis of certain medications. Its chemical properties allow for the development of compounds with specific therapeutic effects, making it an essential component in drug manufacturing processes.
Used in Agrochemical Industry:
2-CHLORO-4-NITRO-N-METHYLANILINE is also utilized as an intermediate in the production of agrochemicals, such as pesticides and herbicides. Its involvement in this industry aids in the development of products designed to protect crops and enhance agricultural productivity.
Environmental Considerations:
Given its potential as an environmental contaminant, 2-CHLORO-4-NITRO-N-METHYLANILINE requires careful management to prevent toxic effects on aquatic organisms. This includes implementing proper disposal methods and containment measures during its production, use, and storage to minimize its release into the environment.
Health and Safety Precautions:
Due to its potential health hazards, it is imperative to exercise caution when handling and storing 2-CHLORO-4-NITRO-N-METHYLANILINE. This includes using appropriate personal protective equipment, ensuring proper ventilation, and adhering to safety guidelines to protect workers and the public from exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 6085-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6085-92:
(6*6)+(5*0)+(4*8)+(3*5)+(2*9)+(1*2)=103
103 % 10 = 3
So 6085-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7ClN2O2/c1-9-7-3-2-5(10(11)12)4-6(7)8/h2-4,9H,1H3

6085-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-4-nitro-<i>N</i>-methylaniline

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-nitro-N-methylaniline

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:6085-92-3 SDS

6085-92-3Relevant academic research and scientific papers

Ortho-halogenated arylamine compound and synthesis method thereof

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Paragraph 0086-0090, (2021/08/06)

The present invention relates to an ortho-halogenated arylamine compound and a synthesis method thereof. The ortho-halogenated arylamine compound has a structure represented by a formula (III), and in the formula (III), X is Cl or Br, Ar is one of substituted naphthyl, phenyl and heteroaryl, and R is one of a benzoyl group, an acetyl group, a pivaloyl group, an ester group, a t-butyloxycarbonyl group, a carbobenzoxy group and a methyl group. According to the invention, cheap and easily available thionyl dihalide reacts with the aryl hydroxylamine compound, efficient synthesis of o-haloarylamine is realized under mild conditions, the universality is good, and various functional groups can well tolerate.

A HIGHLY EFFICIENT AND GENERAL N-MONOMETHYLATION OF FUNCTIONALIZED PRIMARY AMINES VIA FORMYLATION -- BORANE:METHYL SULFIDE REDUCTION

Krishnamurthy, S.

, p. 3315 - 3318 (2007/10/02)

Formylation of functionalized primary aromatic and aliphatic amines with acetic formic anhydride (AFA) followed by borane:methyl sulfide reduction in the same pot affords the corresponding N-methylamines in excellent isolated yields, uncontaminated by bis alkylation; the reaction sequence is applicable to even very weakly basic and sterically hindered amines.

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