CAS 96-99-1

4-Chloro-3-nitrobenzoic acid

Description:

4-Chloro-3-nitrobenzoic acid is an aromatic carboxylic acid characterized by the presence of both a chloro and a nitro group on the benzene ring. Its molecular formula is C7H4ClN1O3, indicating the presence of seven carbon atoms, four hydrogen atoms, one chlorine atom, one nitrogen atom, and three oxygen atoms. This compound typically appears as a yellow crystalline solid and is known for its moderate solubility in organic solvents and limited solubility in water. The chloro and nitro substituents contribute to its reactivity, making it useful in various chemical syntheses, particularly in the production of pharmaceuticals and agrochemicals. 4-Chloro-3-nitrobenzoic acid can undergo typical reactions of carboxylic acids, such as esterification and amidation, and its nitro group can participate in electrophilic aromatic substitution reactions. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate protective equipment should be used.

Formula: C₇H₄ClNO₄

InChI: InChI=1/C7H4ClNO4/c8-5-2-1-4(7(10)11)3-6(5)9(12)13/h1-3H,(H,10,11)/p-1

InChI key: InChIKey=DFXQXFGFOLXAPO-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=CC(C(O)=O)=CC=C1Cl

Synonyms:

• 3-Nitro-4-Chloro Benzoic Acid
• 3-Nitro-4-chlorobenzoic acid
• 4-Chloro-3-Nitobenzoic Acid
• 4-Chloro-3-Nitro Benzoic Acid
• 4-Chloro-3-Nitro-Benzoicacid
• 4-Chloro-3-Nitrobenzoate
• 6-Chloro-3-carboxynitrobenzene
• Benzoic Acid, 4-Chloro-3-Nitro-
• Chloro(4-)-3-Nitrobenzoic Acid
• Labotest-Bb Lt00013440
• NSC 8440
• Rarechem Al Bo 0284
• Timtec-Bb Sbb000404
• 4-Chloro-3-nitrobenzoic acid
• 4-CHLORO-3-NITROBENZOIC ACID GRADE A
• Kyselina 4-chloro-3-nitrobenzoova
• 4-Chloro-3-NitrobenzoicAcid,>99%
• 4-chloro-3-nitro-benzoicaci
• 4-Chloro-3-nitrobenzoic
• 3-nitro-4-Chorobenzoic Acid
• 4-CHLORO-3-NITROBENZOIC ACID GRADE B
• 4-Chloro-3-Nitrobenzoic acid 3-Nitro-4-Chlorobenzoic acid
• kyselina4-chloro-3-nitrobenzoova
• 4-CHLORO-3-NITROBENZOIC ACIC
• 4-Chloro-3-nitrobenzoic acid, 99.5%

4-Chloro-3-nitrobenzoic acid, 10mM (in DMSO)

CAS: 96-99-1

4-Chloro-3-nitrobenzoic acid, 10mM (in DMSO)

Formula: C₇H₄ClNO₄

Purity: ≥98%, 10 mM in DMSO

Molecular weight: 201.56

Ref: 54-BUP18902

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

4-Chloro-3-nitrobenzoic acid

Formula: C₇H₄ClNO₄

Purity: 98%

Color and Shape: Pale yellow Solid-Powder

Molecular weight: 201.56396

Ref: 54-OR51729

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

4-Chloro-3-nitrobenzoic acid

Formula: C₇H₄ClNO₄

Purity: 98+%

Molecular weight: 201.56

Ref: IN-DG01423715

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Purity: %

Color and Shape: Solid

Molecular weight: 201.5640

Ref: IN-DA003L56

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Molecular weight: 201.57

Ref: 7W-GK9450

Proparacaine Impurity 10

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Molecular weight: 201.56

Ref: 4Z-P-305011

4-Chloro-3-nitrobenzoic Acid

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Purity: >98.0%(GC)(T)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 201.56

Ref: 3B-C0223

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

4-Chloro-3-nitrobenzoic acid: aromatic organic, nitric oxide scavenger, studied for cardiovascular and immune system effects.

Formula: C₇H₄ClNO₄

Purity: 99.83% - 99.9%

Color and Shape: White To Pale-Yellow Powder Or Crystals

Molecular weight: 201.56

Ref: TM-T9442

Proparacaine Impurity 10

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Molecular weight: 201.56

Ref: ST-EA-CP-P121024

4-Chloro-3-nitrobenzoic Acid

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Molecular weight: 201.6

Ref: ST-EA-CP-D5101

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

4-Chloro-3-nitrobenzoic acid is a solute that reacts with sodium hydroxide to form 4-chloro-3-nitrophenolate. It also reacts with hydrogen chloride to form 4-chloro-3-nitrobenzoyl chloride. The solubility of the compound in different solvents can be determined by experimental solubility data and structural analysis. 4-Chloro-3-nitrobenzoic acid has been shown to inhibit protein synthesis in liver cells, which may be due to its ability to bind copper ions and form a complex that inhibits the activity of copper enzymes. This compound may also react with sodium salts in the presence of heat or light, leading to the formation of an insoluble precipitate. When heated with strong acids such as hydrogen chloride, 4-chloro-3 nitrobenzoic acid reacts with benzene and forms 3,4 dinitrobenezene

Formula: C₇H₄ClNO₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 201.56 g/mol

Ref: 3D-FC64193

4-Chloro-3-nitrobenzoic acid

CAS: 96-99-1

Formula: C₇H₄ClNO₄

Purity: 95%

Color and Shape: Light yellow powder

Molecular weight: 201.56

Ref: 10-F079099