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2-AMINO-5-CHLORO-3-NITROBENZOIC ACID is a chemical compound with the molecular formula C7H5ClN2O4, belonging to the benzoic acid derivatives. It features an amino group and a nitro group, along with a chlorine atom on the benzene ring, which imparts unique properties and reactivity to the molecule. 2-AMINO-5-CHLORO-3-NITROBENZOIC ACID serves as a crucial intermediate in the chemical and pharmaceutical industries, particularly for the synthesis of pharmaceuticals and organic compounds.

6324-51-2

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6324-51-2 Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-5-CHLORO-3-NITROBENZOIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, 2-AMINO-5-CHLORO-3-NITROBENZOIC ACID is utilized as a building block for the creation of complex organic compounds. Its reactivity and functional groups make it a valuable component in the synthesis of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 6324-51-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6324-51:
(6*6)+(5*3)+(4*2)+(3*4)+(2*5)+(1*1)=82
82 % 10 = 2
So 6324-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClN2O4/c8-3-1-4(7(11)12)6(9)5(2-3)10(13)14/h1-2H,9H2,(H,11,12)

6324-51-2SDS

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 2-amino-5-chloro-3-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 5-Chloro-3-nitroanthranilic acid

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:6324-51-2 SDS

6324-51-2Relevant articles and documents

Composition containing pyridalyl and tolfenpyrad

-

, (2021/09/08)

The invention discloses a composition containing pyridalyl and tetratolfenpyrad, and belongs to the technical field of pesticide synthesis. The composition comprises the following raw materials by weight: 1-50% of pyridalyl, 1-50% of tetratolfenpyrad, 5-15% of a synergist, 0.1-3% of polyethylene glycol, and the balance of water; wherein the pyridalyl and the tetratolfenpyrad have a certain insecticidal effect, a synergist is prepared in the preparation process of the composition, the synergist is used for reducing an intermediate 6 to prepare an intermediate 7, the intermediate 7 reacts with phosgene to prepare an intermediate 8, the intermediate 8 reacts with 2, 2, 2-trifluoroethanol to prepare an intermediate 9, the intermediate 9 is subjected to microspheroidizing treatment; and thus, the synergist is prepared, the synergist can block nerve conduction to enable insects to die, then the insecticidal effect of the composition is further improved, and the pesticide effect is further prolonged through microspheroidizing.

COMPOUNDS USEFUL AS ANTIBIOTIC TOLERANCE INHIBITORS

-

Page/Page column 67, (2014/11/13)

The disclosure provides compounds and pharmaceutical compositions of the compounds useful for treating chronic and acute bacterial infections. Certain of the compounds are compounds and salts of general Formula VIII Certain compounds of this disclosure are MvfR inhibitors. MvfR inhibitors reduce the formation of antibiotic tolerant bacterial strains and are useful for treating Gram-negative bacterial infections and reducing the virulence of Pseudomonas aeruginosa. Methods of treating bacterial infections in a patient, including Pseudomonas aeruginosa infections, are also provided by the disclosure.

Fluoroalkyl-substituted 2-amidobenzimidazoles and their effect on plant growth

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Paragraph 0062-0063, (2013/03/26)

Use of fluoroalkyl-substituted 2-amidobenzimidazoles of the formula (I), or agriculturally acceptable salts thereof, for the treatment of plants for inducing growth regulating responses on plants, on seeds from which they grow or on the locus in which they grow in their normal habitat and in the absence of extraordinary environmental conditions and which result in superior growth of these treated plants, certain parts of these plants or, more generally, crop yield.

Fluoroalkyl-substituted 2-amidobenzimidazoles

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Page/Page column 13, (2011/10/02)

Use of fluoroalkyl-substituted 2-amidobenzimidazoles of the formula (I), or salts thereof, for enhancing stress tolerance in plants to abiotic stress, especially for strengthening plant growth and/or for increasing plant yield, and selected processes for preparing such fluoroalkyl-substituted 2-amidobenzimidazoles of the formula (I).

DIHYDROOROTATE DEHYDROGENASE INHIBITORS

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Page/Page column 96, (2010/11/03)

The invention relates to compounds of formula (I) wherein R1, R2, X1, X2, Y, Ra, Rb, Q have the meanings given in claim 1. The compounds are useful e.g. in the treatment of autoimmune disorders, such as multiple sclerosis and also in the treatment of cancer disorders.

Process development for ABT-472, a benzimidazole PARP inhibitor

Barkalow, Jufang H.,Breting, Jeffrey,Gaede, Bruce J.,Haight, Anthony R.,Henry, Rodger,Kotecki, Brian,Mei, Jianzhang,Pearl, Kurt B.,Tedrow, Jason S.,Viswanath, Shekhar K.

supporting information, p. 693 - 698 (2012/12/29)

A nine-step convergent process was developed for the synthesis of ABT-472, a benzimidazole PARP inhibitor. The identity and origin of several impurities were determined, and the process was modified to reduce or eliminate these impurities. A number of safety and control issues were investigated. The original synthesis was shortened to 9 steps and streamlined while maintaining a convergent strategy. A stable salt was selected, and control of the API solid form was established. The process was successfully scaled up to provide 8.5 kg of final product of >99% purity in 33% yield over 9 steps.

Synthesis and SAR of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones related to licostinel (Acea 1021) as NMDA/glycine site antagonists

Zhou, Zhang-Lin,Kher, Sunil M.,Cai, Sui Xiong,Whittemore, Edward R.,Espitia, Stephen A.,Hawkinson, Jon E.,Tran, Minhtam,Woodward, Richard M.,Weber, Eckard,Keana, John F. W.

, p. 1769 - 1780 (2007/10/03)

A series of novel di- and trisubstituted 1,4-dihydroquinoxaline-2,3-diones (QXs) related to licostinel (Acea 1021) was synthesized and evaluated as antagonists for the glycine site of the N-methyl-D-asparate (NMDA) receptor. The in vitro potency of these

Fused Tetracyclic quinoxalines from reactions of o-phenylenediamines in polyphosphoric acid

Deady, Leslie W.,Kaye, Anthony J.

, p. 473 - 478 (2007/10/03)

The condensation of 2,3-diaminobenzoic acid and the 5-chloro derivative with o-hydroxyphenylglyoxylic acid, isatin and benzothiophen-2,3-dione in polyphosphoric acid leads to the appropriate tetracycles. Isomeric products are formed from these unsymmetric

(R)-3-(6-chloro-1-isopropylbenzimidazole-4-carboxamido)quinuclidine: A high affinity ligand for the (R)-zacopride binding site

Flippin,Carter,Berger,Clark,Bonhaus,Leung,Eglen

, p. 477 - 480 (2007/10/03)

The (R)-3-amido quinuclidine 6 (RS-16566) was found to be a high affinity ligand for the (R)-zacopride binding site.

Process for preparing 5-halo-2,3-phenylenediamine-1-carboxylic acid

-

, (2008/06/13)

Method of preparing 5-halo-2,3-phenylenediamine-1-carboxylic acids having the following formula: SPC1 Wherein X is Cl, Br or F by reacting a 2,5-dihalo-3-nitrobenzoic acid with ammonium hydroxide to yield 5-halo-3-nitro anthranilic acid followed by a redu

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