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Methyl 3-chloro-5-nitrobenzoate is a scientific compound with the formula C8H6ClNO4. It belongs to the class of organic compounds known as nitrobenzenes, which are compounds containing a nitrobenzene moiety, consisting of a benzene ring with a nitro group (NO2) attached to it. This specific chemical features two such groups, as well as a methyl ester group (COOCH3), attached to its benzene ring. Although it has varying uses in chemical industries, limited information is present regarding its safety and environmental properties. Like other nitro compounds, it is likely to be highly reactive and may pose hazards if improperly handled or disposed of.

36138-28-0

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36138-28-0 Usage

Uses

Used in Chemical Industries:
Methyl 3-chloro-5-nitrobenzoate is used as a chemical intermediate for the synthesis of various compounds in the chemical industry. Its presence of nitro and chloro groups, along with the methyl ester, makes it a versatile building block for the creation of a wide range of products.
Used in Research and Development:
Methyl 3-chloro-5-nitrobenzoate is used as a research compound in academic and industrial laboratories. Its unique structure and reactivity make it a valuable tool for studying the properties and reactions of nitrobenzenes and related compounds, contributing to the advancement of chemical knowledge and technology.
Used in Pharmaceutical Industry:
Methyl 3-chloro-5-nitrobenzoate is used as a starting material in the synthesis of pharmaceutical compounds. Its potential to be transformed into various drug molecules makes it an important component in the development of new medications and therapies.
Used in Dye and Pigment Production:
Methyl 3-chloro-5-nitrobenzoate is used as a raw material in the production of dyes and pigments. Its chemical structure allows for the creation of a variety of colors and shades, making it a valuable resource in the manufacturing of paints, inks, and other colorants.

Check Digit Verification of cas no

The CAS Registry Mumber 36138-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,3 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36138-28:
(7*3)+(6*6)+(5*1)+(4*3)+(3*8)+(2*2)+(1*8)=110
110 % 10 = 0
So 36138-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO4/c1-14-8(11)5-2-6(9)4-7(3-5)10(12)13/h2-4H,1H3

36138-28-0SDS

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 Methyl 3-chloro-5-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 3-chloro-5-nitro-benzoic acid methyl ester

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:36138-28-0 SDS

36138-28-0Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 273-274, (2020/07/06)

Herein, compounds, compositions and methods for modulating inclusion formation and stress granules in cells related to the onset of neurodegenerative diseases, musculoskeletal diseases, cancer, ophthalmological diseases, and viral infections are described.

QUINAZOLINE DERIVATIVES AS ANTIVIRAL AGENTS

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Page/Page column 35, (2010/11/26)

The present invention relates to the use of quinazoline derivatives of formula (I) wherein A, B, R1, R2, R3 and R4 are defined herein, and pharmaceutically acceptable salts thereof, for the treatment or preventi

PYRROLE DERIVATIVES WITH CRTH2 RECEPTOR MODULATOR ACTIVITY

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Page/Page column 37, (2008/06/13)

There are provided according to the invention compounds of formula (I) in free or salt form, wherein R3, R 4, R5, R6a, R6b, Q and W are as described in the specification, process for preparing them, a

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