18985-99-4

Upstream product

• 108-94-1 cyclohexanone 
• 91-00-9 Benzhydrylamine 
• 119-61-9 benzophenone 
• 5267-34-5 aminodiphenylmethane hydrochloride 

Downstream Products

• 30857-82-0 3,3-diphenyl-1,2-dioxa-4-aza-spiro[4.5]decane 
• 65577-27-7 [1-(Benzhydryl-amino)-cyclohexyl]-phosphinic acid 
• 65576-91-2 (1-Amino-cyclohexyl)-phosphinic acid 
• 735-11-5 N-(diphenylmethyl)cyclohexanamine 
• 16770-34-6 N-(α-phenylbenzylidene)cyclohexylamine 

Relevant academic research and scientific papers

Benzhydrylamine: An effective aminating agent for the synthesis of primary amines

Aldehydes, ketones, alkyl toluene-p-sulfonates and halides are converted into the corresponding primary amines with benzhydrylamine as a valuable ammonia synthon in moderate to excellent yields.

Determination of the conformations and relative configurations of exocyclic amines

The conformations and relative configurations of 20 amines, classified according to the following labeling scheme, were analyzed. Series a comprised compounds derived from N-(1-phenylethyl)cyclohexanamine, b comprised derivatives of N-[1-(naphthalen-2-yl)ethyl]cyclohexanamine, c comprised derivatives of N-(diphenylmethyl)cyclohexanamine, and d comprised derivatives of N-(propan-2-yl)cyclohexanamine. The compounds were labeled as follows: 1 indicates cyclohexanamine, 2 indicates 2-methylcyclohexanamines, 3 indicates 3-methylcyclohexanamines, 4 indicates 4-methylcyclohexanamines, and 5 indicates 4-tert-butylcyclohexanamines. These compounds were prepared without the use of stereoselective induction and, therefore, all expected stereoisomers were observed. Structural assignments were established by 1H, 13C, and 15N NMR.

α-Amino-phosphonous acids for inhibiting bacteria and yeast

The present invention relates to new phosphonous acid derivatives, especially to α-amino-phosphonous acids and processes for their production. The new phosphonous acids are valuable chemotherapeutica in the treatment of pathogenic bacteria, gram-negative