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2,5-DIMETHYL-3-NITROBENZOIC ACID is a chemical compound characterized by the molecular formula C9H9NO4. It is a member of the benzoic acid class, featuring a nitro group and two methyl groups attached to the benzene ring. 2,5-DIMETHYL-3-NITROBENZOIC ACID is recognized for its role as a synthetic intermediate in various industrial applications, including the production of pharmaceuticals, agrochemicals, dyes, pigments, and in organic synthesis. Furthermore, it holds potential in the realm of materials science and polymers. Due to its potential health hazards, it is crucial to handle 2,5-DIMETHYL-3-NITROBENZOIC ACID with appropriate safety measures.

27022-97-5

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27022-97-5 Usage

Uses

Used in Pharmaceutical Industry:
2,5-DIMETHYL-3-NITROBENZOIC ACID is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical structure allows it to serve as a building block in the synthesis of drug molecules, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,5-DIMETHYL-3-NITROBENZOIC ACID is utilized as a precursor in the synthesis of agrochemicals. Its properties make it suitable for the development of compounds used in crop protection and other agricultural applications.
Used in Dye and Pigment Industry:
2,5-DIMETHYL-3-NITROBENZOIC ACID is employed in the preparation of dyes and pigments due to its chemical composition. It plays a role in creating colorants used in various industries, such as textiles, plastics, and printing inks.
Used in Organic Synthesis:
2,5-DIMETHYL-3-NITROBENZOIC ACID is used as a reactant in organic synthesis, where it can be transformed into other chemical entities through various chemical reactions. Its versatility in synthesis makes it valuable in the creation of a wide range of organic compounds.
Used in Materials Science and Polymers:
2,5-DIMETHYL-3-NITROBENZOIC ACID has potential applications in the field of materials science, particularly in the development of new polymers and materials with unique properties. Its incorporation into these materials can lead to advancements in material performance and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 27022-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,2 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27022-97:
(7*2)+(6*7)+(5*0)+(4*2)+(3*2)+(2*9)+(1*7)=95
95 % 10 = 5
So 27022-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-5-3-7(9(11)12)6(2)8(4-5)10(13)14/h3-4H,1-2H3,(H,11,12)

27022-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethyl-3-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Nitro-2,5-dimethyl-benzoesaeure

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:27022-97-5 SDS

27022-97-5Upstream product

27022-97-5Downstream Products

27022-97-5Relevant academic research and scientific papers

HETEROAROMATIC MODULATORS OF THE RETINOID-RELATED ORPHAN RECEPTOR GAMMA

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Page/Page column 38; 46; 47, (2018/03/28)

The present invention relates to a compound according to general formula (I) wherein X represents N or CH; R1 is -CN, (C1-C6)alkyl, (C3-C7)cycloalkyl, (3-7 membered)heterocycloalkyl, (5-6 membered)heteroaryl, (C3-C7)cycloalkyl(C1-C4)alkyl, (3-7 membered)heterocycloalkyl-(C1-C4)alkyl or (5-6 membered)heteroaryl- (C1-C4)alkyl; R2 is halogen, cyano, (C1-C4)alkyl or (C3-C7)cycloalkyl; R3 is halogen, cyano, (C1-C4)alkyl, (C1-C4)haloalkyl or (C3-C7)cycloalkyl; R4 is (C1-C4)alkyl or (C1-C4)haloalkyl; R5 is (C1-C6)alkyl, (C3-C7)cycloalkyl, (C1-C6)alkyl-(C3-C7)cycloalkyl, (C3-C7)cycloalkyl-(C1-C6)alkyl, (3-7 membered)heterocycloalkyl, phenyl, (5-6 membered)heteroaryl or -ORa. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds and to intermediates for preparation of said compounds.

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