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

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

Downstream Products

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

Relevant articles and documents

Screening of simple carbohydrates as a renewable organocatalyst for the efficient construction of 1,3-benzoxazine scaffold

A convenient protocol for the two component preparation of 1,3-benzoxazines by using several protected and unprotected carbohydrate molecules as organocatalysts have been developed which is broadly applicable to condensation reaction between variety of Ma

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-

Aminophenols as efficient ligand for copper-Catalyzed ullmann-Type synthesis of diaryl ethers

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