CAS 22996-18-5

4-Chloro-2-nitrobenzenemethanol

Description:

4-Chloro-2-nitrobenzenemethanol, with the CAS number 22996-18-5, is an organic compound characterized by the presence of a chlorinated and nitro-substituted benzene ring attached to a hydroxymethyl group. This compound typically appears as a solid at room temperature and is soluble in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The chlorinated and nitro groups contribute to its reactivity, making it a potential intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The presence of the nitro group often imparts electrophilic characteristics, while the chloro group can facilitate nucleophilic substitution reactions. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 4-Chloro-2-nitrobenzenemethanol is a valuable compound in synthetic organic chemistry, with applications that leverage its unique functional groups.

Formula: C₇H₆ClNO₃

InChI: InChI=1S/C7H6ClNO3/c8-6-2-1-5(4-10)7(3-6)9(11)12/h1-3,10H,4H2

InChI key: InChIKey=OAHGNOHGHOTZQU-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=C(CO)C=CC(Cl)=C1

Synonyms:

• (4-Chloro-2-Nitrophenyl)Methanol
• (4-Chloro-3-Nitrophenyl)Methanol
• 4-Chloro-2-nitrobenzenemethanol
• Benzenemethanol, 4-chloro-2-nitro-
• Benzyl alcohol, 4-chloro-2-nitro-
• 4-Chloro-2-nitrobenzyl alcohol

(4-Chloro-2-nitrophenyl)methanol

CAS: 22996-18-5

Formula: C₇H₆ClNO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 187.5804

Ref: IN-DA003L41

4-Chloro-2-nitrobenzyl alcohol

CAS: 22996-18-5

Ref: 7W-GK2424

4-Chloro-2-nitrobenzyl alcohol

CAS: 22996-18-5

4-Chloro-2-nitrobenzyl alcohol

Formula: C₇H₆ClNO₃

Purity: 97%

Color and Shape: beige solid

Molecular weight: 187.58g/mol

Ref: 54-OR401026

4-Chloro-2-nitrobenzyl alcohol

CAS: 22996-18-5

Formula: C₇H₆ClNO₃

Purity: 97%

Molecular weight: 187.58

Ref: 10-F237388

4-Chloro-2-nitrobenzyl alcohol

CAS: 22996-18-5

4-Chloro-2-nitrobenzyl alcohol is an organic compound that is a reactive nucleophile and isomer. It undergoes slow reactions with water and other nucleophiles. The reactivity of 4-chloro-2-nitrobenzyl alcohol is dependent on the solvent, pH, and temperature. This chemical does not react with most substances, including proteins and carbohydrates. 4-Chloro-2-nitrobenzyl alcohol inhibits the growth of bacteria by reacting with bacterial cytoplasmic membrane lipids, which disrupts its integrity. 4-Chloro-2-nitrobenzyl alcohol also inhibits the synthesis of proteins in bacterial cells by binding to ribosomes and interfering with translation.

Formula: C₇H₆ClNO₃

Purity: Min. 95%

Molecular weight: 187.58 g/mol

Ref: 3D-XAA99618