7278-77-5

Basic information

• Product Name: (1-chloro-cycloheptyl)-phenyl-methanone
• Synonyms: (1-chloro-cycloheptyl)-phenyl-methanone
• CAS NO: 7278-77-5
• Molecular Weight: 236.741
• Mol File: 7278-77-5.mol

Chemical Properties

• CAS DataBase Reference: (1-chloro-cycloheptyl)-phenyl-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1-chloro-cycloheptyl)-phenyl-methanone(7278-77-5)
• EPA Substance Registry System: (1-chloro-cycloheptyl)-phenyl-methanone(7278-77-5)

Safety Data

• Hazardous Substances Data: 7278-77-5(Hazardous Substances Data)

Upstream product

• 32730-85-1 cycloheptanecarbonitrile 
• 100-58-3 phenylmagnesium bromide 
• 98-07-7 Benzotrichlorid 
• 502-42-1 cycloheptanone 

Downstream Products

• 1196090-71-7 (R)-1-(benzo[d]isoxazol-3-ylcarbamoylmethyl)-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane chloride 
• 1196091-68-5 (R)-1-(oxazol-2-ylcarbamoylmethyl)-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane bromide 
• 1196091-50-5 (R)-1-[(Methyl-phenyl-carbamoyl)-methyl]-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane formate 
• 1196091-43-6 (R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane formate 
• 1196093-11-4 1-phenyl-cycloheptanecarboxylic acid (S)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester 
• 1196091-31-2 (R)-3-(1-phenyl-cycloheptanecarbonyloxy)-1-(2-pyrazin-2-yl-ethyl)-azonia-bicyclo[2.2.2]octane bromide 
• 1196091-20-9 (R)-3-(1-phenyl-cycloheptanecarbonyloxy)-1-(pyridazin-4-ylcarbamoylmethyl)-1-azonia-bicyclo[2.2.2]octane formate 
• 1026791-31-0 1-phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester 
• 1196091-89-0 (R)-3-(1-Phenyl-cycloheptanecarbonyloxy)-1-(3-pyridin-4-yl-propyl)-1-azonia-bicyclo[2.2.2]octane bromide 
• 1196091-88-9 (R)-3-(1-Phenyl-cycloheptanecarbonyloxy)-1-{2-[(pyridine-2-carbonyl)-amino]-ethyl}-1-azonia-bicyclo[2.2.2]octane bromide 
• 1196091-85-6 (R)-1-[(6-Methyl-pyrimidin-4-ylcarbamoyl)-methyl]-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane chloride 
• 1196091-83-4 (R)-1-[(2-Methyl-pyrimidin-4-ylcarbamoyl)-methyl]-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane chloride 
• 1196091-82-3 (R)-3-(1-Phenyl-cycloheptanecarbonyloxy)-1-{3-[(pyridine-2-carbonyl)-amino]-propyl}-1-azonia-bicyclo[2.2.2]octane bromide 
• 1196090-64-8 (R)-1-[(6-Methyl-pyridin-3-ylcarbamoyl)-methyl]-3-(1-phenyl-cycloheptanecarbonyloxy)-1-azonia-bicyclo[2.2.2]octane chloride 

Relevant articles and documents

QUINUCLIDINE DERIVATIVES AS MUSCARINIC M3 RECEPTOR ANTAGONISTS

The invention provides named compounds of formula (I), wherein R4 is a N-substituted quinuclidine (I) pharmaceutical compositions containing them and a process for preparing the pharmaceutical compositions. Their use in therapy for’ the treatment of conditions mediated by M3 muscarinic receptors, such as chronic obstructive pulmonary disease is also disclosed.

1,2-Addition of α,α,α-trichlorotoluene to ketones via a Mg Barbier reaction in DMF: New route to cycloalk-1-en-1-yl and alk-1-en-1-yl phenyl ketones

The reductive cyclocondensation of α,α,α-trichlorotoluene to enolisable ketones enables the preparation of (cyclo)alken-1-en-1-yl phenyl ketones via the formation of an intermediate chlorooxirane. Copyright Taylor & Francis Group, LLC.