40256-25-5

Basic information

• Product Name: 2-(1-Benzyl-piperidin-4-yloxy)-ethanol
• Synonyms: 2-(1-Benzyl-piperidin-4-yloxy)-ethanol
• CAS NO: 40256-25-5
• Molecular Formula: C₁₄H₂₁NO₂
• Molecular Weight: 235.32204
• Mol File: 40256-25-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(1-Benzyl-piperidin-4-yloxy)-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-Benzyl-piperidin-4-yloxy)-ethanol(40256-25-5)
• EPA Substance Registry System: 2-(1-Benzyl-piperidin-4-yloxy)-ethanol(40256-25-5)

Safety Data

• Hazardous Substances Data: 40256-25-5(Hazardous Substances Data)

Upstream product

• 37943-54-7 8-benzyl-1,4-dioxa-8-azaspiro[4.5]decane 
• 4727-72-4 1-benzyl-4-hydroxypiperidine 
• 67385-09-5 2-[(tert-butoxycarbonyl)amino]-1-ethanethiol 

Relevant articles and documents

INDOLE DERIVATIVES AS ESTROGEN RECEPTOR DEGRADERS

The present disclosure relates to compounds and a pharmaceutically acceptable salt thereof, compositions, combinations and medicaments containing the compounds, and processes for their preparation. The disclosure also relates to the use of the compounds, combinations, compositions and medicaments, for example as inhibitors of the activity of the estrogen receptor, including degrading the estrogen receptor, the treatment of diseases and conditions mediated by the estrogen receptor.

10-(Piperidin o-alkyl)-phenothiazines

Novel 10-(piperidino-alkyl)-phenothiazines of the formula STR1 wherein X is selected from the group consisting of hydrogen, chlorine, --CF3, --OCH3 and SCH3, B and R are individually selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, Z' is selected from the group consisting of hydrogen and alkyl of 1 to 10 carbon atoms, p is 0 or 1, n is 0, 1 or 2 and A is selected from the group consisting of hydrogen, --COOR2 and --COR1, R2 is linear alkyl of 1 to 15 carbon atoms and R1 is selected from the group consisting of alkyl of 1 to 18 carbon atoms optionally containing a double bond or --O-- and a polymethoxyphenyl and their non-toxic, pharmaceutically acceptable acid addition salts having neuroleptic, analgesic, spasmolytic and antihistaminic activity and their preparation and novel intermediates.