1159372-20-9

Basic information

• Product Name: (2-amino-5-chlorophenyl)(phenyl)methanol
• Synonyms: (2-amino-5-chlorophenyl)(phenyl)methanol
• CAS NO: 1159372-20-9
• Molecular Weight: 233.697
• Mol File: 1159372-20-9.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: (2-amino-5-chlorophenyl)(phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2-amino-5-chlorophenyl)(phenyl)methanol(1159372-20-9)
• EPA Substance Registry System: (2-amino-5-chlorophenyl)(phenyl)methanol(1159372-20-9)

Safety Data

• Hazardous Substances Data: 1159372-20-9(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 106-47-8 4-chloro-aniline 
• 20028-53-9 2-amino-5-chlorobenzaldehyde 
• 100-58-3 phenylmagnesium bromide 
• 6628-86-0 5-chloro-2-nitrobenzaldehyde 
• 60794-27-6 (5-chloro-2-nitro-phenyl)-phenyl-methanol 
• 719-59-5 5-chloro-2-aminobenzophenone 

Downstream Products

• 40545-76-4 2-Amino-5-chlordiphenylmethan 
• 22609-01-4 ethyl 6-chloro-2-methyl-4-phenylquinoline-3-carboxylate 
• 121659-89-0 ethyl 6-chloro-2,4-diphenylquinoline-3-carboxylate 
• 64820-66-2 6-chloro-4-phenyl-3,4-dihydro-1H-quinazolin-2-one 
• 132735-16-1 6-Chloro-3,4-diphenyl-2-thioxo-1,2,3,4-tetrahydroquinazoline 
• 13213-86-0 6-chloro-4-phenyl-1,4-dihydro-2H-3,1-benzoxazin-2-one 
• 13540-41-5 6-chloro-4-phenyl-1,4-dihydro-benzo[d][1,3]oxazine-2-thione 

Relevant articles and documents

An efficient iron-promoted synthesis of 6H-indolo[2,3- b] quinolines and neocryptolepine derivatives

A facile and practical method for the preparation of 6H-indolo[2,3-b]quinolines and neocryptolepines was developed under the promotion of the easily available ferric trichloride, affording the desired products with moderate to good yields.

Facile Access to Triazole-Fused 3,1-Benzoxazines Enabled by Metal-Free Base-Promoted Intramolecular C-O Coupling

A convenient approach to assemble 1,2,3-triazole-fused 4 H -3,1-benzoxazines has been developed. Diverse alcohol-tethered 5-iodotriazoles, readily accessible by a modified protocol of Cu-catalyzed (3+2)-cycloaddition, were utilized as precursors of the target fused heterocycles. The intramolecular C-O coupling proceeded efficiently under base-mediated transition-metal-free conditions, furnishing cyclization products in yields up to 96%. Suppression of the competing reductive cleavage of the C-I bond was achieved by the use of Na 2CO 3in acetonitrile at 100 °C. This practical and cost-effective procedure features a broad substrate scope and valuable functional group tolerance.

Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity

A novel metal-free intramolecular oxidative decarboxylative coupling of primary α-amino acids with 2-aminobenzoketones under mild and neutral conditions was developed. Different quinazolines can be selectively obtained by various oxidants.