10254-07-6

Basic information

• Product Name: N-Benzhydryl-2-chloro-acetamide
• Synonyms: N-Benzhydryl-2-chloro-acetamide;2-chloro-N-(diphenylmethyl)acetamide;2-chloro-N-[di(phenyl)methyl]acetamide;2-chloro-N-[di(phenyl)methyl]ethanamide
• CAS NO: 10254-07-6
• Molecular Formula: C₁₅H₁₄ClNO
• Molecular Weight: 259.74
• Mol File: 10254-07-6.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Benzhydryl-2-chloro-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzhydryl-2-chloro-acetamide(10254-07-6)
• EPA Substance Registry System: N-Benzhydryl-2-chloro-acetamide(10254-07-6)

Safety Data

• Hazardous Substances Data: 10254-07-6(Hazardous Substances Data)

Upstream product

• 79-04-9 chloroacetyl chloride 
• 91-00-9 Benzhydrylamine 
• 100-52-7 benzaldehyde 
• 79-07-2 Chloroacetamide 
• 98-80-6 phenylboronic acid 
• 574-66-3 Benzophenone oxime 
• 91-01-0 1,1-Diphenylmethanol 
• 107-14-2 chloroacetonitrile 
• 79-11-8 chloroacetic acid 

Downstream Products

• 110330-55-7 (1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-purin-7-yl)-acetic acid benzhydrylamide 
• 59960-80-4 N-<(N',N'-diethylamino)acetyl>diphenylmethylamine 
• 1000291-17-7 C₃₁H₂₈N₄O₂S 
• 1000291-23-5 C₃₁H₃₄N₄O₂S 
• 957758-48-4 C₃₂H₃₆N₄O₂S 
• 957758-52-0 C₃₁H₂₇ClN₄O₂S 
• 841241-96-1 N-(benzhydryl)-2-(2-methylpiperidin-1-yl)acetamide 
• 1008017-89-7 N-(benzhydryl)-2-(3-methylpiperidin-1-yl)acetamide 
• 604762-55-2 N-(benzhydryl)-2-(4-methylpiperidin-1-yl)acetamide 
• 838090-86-1 N-(benzhydryl)-2-(3,5-dimethylpiperidin-1-yl)acetamide 
• 1429426-56-1 N-(benzhydryl)-2-(2,6-dimethylpiperidin-1-yl)acetamide 
• 1155875-02-7 N-diphenylmethyl-1,2-dichloroacetylimine 
• 258532-90-0 N-diphenylmethyl-2-(8-hydroxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-4-yl)acetamide 

Relevant articles and documents

Silica gel supported ferric perchlorate: A new and efficient reagent for one pot synthesis of amides from benzylic alcohols

Benzylic alcohols react efficiently with nitriles in the presence of silica gel supported ferric perchlorate to produce amides in high yields.

Synthesis of some dithiocarbamate derivatives and their antimicrobial activity

Some new, 2-[(N-substituted aminothiocarbonylthio)acetyl]aminothiazole, N-substituted aminothiocarbonylthioacetylaminodiphenylmethane and 9-[(N-substituted aminothiocarbonylthio)acetyl]aminofluorene derivatives were synthesized by reacting 2-(chloroacetyl

Method for synthesizing amide compound by taking nitrile and diaryl methane as raw materials

The invention discloses a method for synthesizing an amide compound by taking nitrile and diaryl methane as raw materials, the method comprises the following steps: taking diaryl methane as a reaction raw material, nitrile as a raw material and a solvent, 2, 3-dichloro-5, 6-dinitrile group-1, 4-benzoquinone (DDQ) and tert-butyl nitrite (TBN) as catalysts, acid as an auxiliary agent and oxygen as an oxidizing agent, reacting under the conditions of normal temperature, normal pressure and blue light irradiation, and after the reaction is finished, carrying out separation treatment to obtain the amide compound. According to the method, the problem of metal residues in the product can be solved, oxygen is used as a terminal oxidizing agent, the method is environmentally friendly, and energy can be saved.

A Lewis acid palladium(II)-catalyzed three-component synthesis of α-substituted amides

A Lewis acid palladium-catalyzed reaction of amides, aryl aldehydes, and arylboronic acids is described. This new method allows for a practical and general synthesis of α-substituted amides from simple, readily available building blocks.

Preparation of different amides via Ritter reaction from alcohols and nitriles in the presence of silica-bonded N-propyl sulphamic acid (SBNPSA) under solvent-free conditions

A number of methods have been proposed for the modification of the Ritter reaction. However, many of these methods involve the use of strongly acidic conditions, stoichiometric amounts of reagents, harsh reaction conditions and extended reaction times. Th