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CAS

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130597-56-7

4-(Chloromethyl)-N-methyl-2-nitroaniline, a chemical compound with the molecular formula C8H9ClN2O2, is a yellow crystalline solid. It has a molecular weight of 204.62 g/mol and is known for its role as an intermediate in the synthesis of pharmaceuticals, agrochemicals, dyes, and pigments. Due to its potential health and environmental risks, it is classified as a hazardous substance that requires careful handling and storage.

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  • 130597-56-7 Structure

  • Basic information

    1. Product Name: 4-(Chloromethyl)-N-methyl-2-nitroaniline
    2. Synonyms: 4-(Chloromethyl)-N-methyl-2-nitroaniline
    3. CAS NO:130597-56-7
    4. Molecular Formula: C8H9ClN2O2
    5. Molecular Weight: 201
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130597-56-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(Chloromethyl)-N-methyl-2-nitroaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(Chloromethyl)-N-methyl-2-nitroaniline(130597-56-7)
    11. EPA Substance Registry System: 4-(Chloromethyl)-N-methyl-2-nitroaniline(130597-56-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 130597-56-7(Hazardous Substances Data)

130597-56-7 Usage

Uses

Used in Pharmaceutical Industry:
4-(Chloromethyl)-N-methyl-2-nitroaniline is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(Chloromethyl)-N-methyl-2-nitroaniline serves as an intermediate in the production of agrochemicals. Its involvement in the synthesis process helps create effective solutions for agricultural applications, such as pesticides and herbicides.
Used in Dye and Pigment Manufacturing:
4-(Chloromethyl)-N-methyl-2-nitroaniline is utilized as a starting material in the manufacturing of dyes and pigments. Its chemical properties make it suitable for creating a wide range of colors used in various industries, including textiles, plastics, and printing inks.
Due to the hazardous nature of 4-(Chloromethyl)-N-methyl-2-nitroaniline, it is crucial to follow proper safety protocols during its handling, storage, and use to minimize potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 130597-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,9 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130597-56:
(8*1)+(7*3)+(6*0)+(5*5)+(4*9)+(3*7)+(2*5)+(1*6)=127
127 % 10 = 7
So 130597-56-7 is a valid CAS Registry Number.

130597-56-7SDS

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 4-(Chloromethyl)-N-methyl-2-nitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-(chloromethyl)-N-methyl-2-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:130597-56-7 SDS

130597-56-7Downstream Products

130597-56-7Relevant articles and documents

Artificial redox enzymes

-

, (2008/06/13)

Artificial redox enzymes are disclosed wherein one or more redox coenzymes or cofactors are linked to the 2-O, 3-O or 6-O positions of a D-glucopyranose ring of α-, β-, or γ-cyclodextrins. Also disclosed are facile synthetic methods for producing said art

Artificial Redox Enzymes. 1. Synthetic Strategies

Rong, Ding,Ye, Hongping,Boehlow, Todd R.,D'Souza, Valerian T.

, p. 163 - 167 (2007/10/02)

Organic models of flavoenzymes consist of a binding site covalently attached to a flavin derivative acting as the catalytic site.The earlier reported synthesis of such a model using α-cyclodextrin as the binding site proved to be difficult to reproduce wi

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