7193-94-4

Basic information

• Product Name: 2-[(4-chloroanilino)methyl]phenol
• Synonyms: 2-[(4-chloroanilino)methyl]phenol;N-(4-Chlorophenyl)-2-hydroxybenzenemethanamine;α-(p-Chloroanilino)-o-cresol;ALPHA-(4-CHLOROANILINO)-ORTHO-CRESOL;o-Cresol, .alpha.(p-chloroanilino)-
• CAS NO: 7193-94-4
• Molecular Formula: C₁₃H₁₂ClNO
• Molecular Weight: 233.7
• Mol File: 7193-94-4.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[(4-chloroanilino)methyl]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-chloroanilino)methyl]phenol(7193-94-4)
• EPA Substance Registry System: 2-[(4-chloroanilino)methyl]phenol(7193-94-4)

Safety Data

• Hazardous Substances Data: 7193-94-4(Hazardous Substances Data)

Usage

Appearance

White to off-white solid

Molecular weight

239.69 g/mol

Usage

Manufacturing of pharmaceuticals, intermediate in organic synthesis

Antimicrobial properties

Acts as an antiseptic and disinfectant

Safety concerns

Known irritant, can cause skin and eye irritation, should be handled with caution

Industrial and medical applications

Versatile chemical used in various industries and medical treatments

Upstream product

• 90-01-7 salicylic alcohol 
• 106-47-8 4-chloro-aniline 
• 90-02-8 salicylaldehyde 
• 29199-18-6 3-(4-methoxyphenyl)pentenedioic anhydride 
• 782-77-4 N-(o-hydroxybenzylidene)-p-chloroaniline 
• 782-77-4 N-(4-chlorophenyl)salicylaldimine 
• 19865-61-3 N-(salicylidene)-4-chlorophenylamine-N-oxide 
• 280-64-8 9-bora-bicyclo[3.3.1]nonane 
• 51892-07-0 3-(4-chlorophenyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 50-00-0 formaldehyd 
• 108-95-2 phenol 

Downstream Products

• 102002-39-1 4-chloro-N,N-disalicyl-aniline 
• 106475-24-5 2-(4-chloro-N-nitroso-anilinomethyl)-phenol 
• 51892-07-0 3-(4-chlorophenyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 1082608-48-7 2-chloro-3-(4-chlorophenyl)-3,4-dihydro-2H-1,3,2λ5-benzoxazaphosphinine-2-thione 
• 1169938-11-7 2,4,6-trinitrobenzoic acid N-(2-hydroxy-benzyl)-4-chloroanilide 
• 1207178-52-6 3-(4-chlorophenyl)-2-(4-nitrophenyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 1207178-41-3 3-(4-chlorophenyl)-2-(2-nitrophenyl)-3,4-dihydro-2H-benzo[e][1,3]oxazine 
• 1222170-26-4 4-(4-chlorophenyl)-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-thione 
• 7034-29-9 4-(4-chlorophenyl)-4,5-dihydrobenzo[f][1,4]oxazepin-3(2H)-one 
• 99779-29-0 2-chloro-N-(2-hydroxybenzyl)-N-(4-chlorophenyl)acetamide 
• 1396314-96-7 2-(4-fluorophenyl)-3-(4-chlorophenyl)-3,4-dihydro-2H-1,3-benzoxazine 
• 1207178-47-9 2-(3-nitrophenyl)-3-(4-chlorophenyl)-3,4-dihydro-2H-1,3-benzoxazine 
• 1396315-00-6 3-(4-chlorophenyl)-2-phenyl-3,4-dihydro-2H-1,3-benzoxazine 
• 67-63-0 isopropyl alcohol 

Relevant articles and documents

A simple method for the reduction of Schiff bases using biosynthesized nickel oxide nanoparticles

An innovative and simple approach for the reduction of aldimines to the corresponding secondary amines was described using biosynthesized nickel oxide nanoparticles as heterogeneous catalyst and ammonium formate as the hydrogen donor. This catalytic trans

Metal-Free Diaryl Etherification of Tertiary Amines by Ortho-C(sp2)-H Functionalization for Synthesis of Dibenzoxazepines and -ones

A phenyliodine(III) diacetate mediated umpolung reactivity of the tertiary amines with suitably substituted o-hydroxybenzyl and phenyl groups is exploited to facilitate o-C(sp2)-H functionalization to afford diaryl ethers. The presence of an o-

A quick route for the synthesis of 3-Aryl-3,4-dihydro-2H-benz[e]-1,3- oxazin-2-ones

N-(2-Hydroxy)-benzyl-arylamines (1) gave substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazin-2-one 2 on cyclization with carbonyldiimidazole in DMSO in 20-30 min at 20-25 °C in excellent yields.