19980-00-8

Basic information

• Product Name: 4-Piperidinemethanol, 1-benzoyl-
• CAS NO: 19980-00-8
• Molecular Formula: C13H17NO2
• Molecular Weight: 219.283
• Mol File: 19980-00-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 4-Piperidinemethanol, 1-benzoyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Piperidinemethanol, 1-benzoyl-(19980-00-8)
• EPA Substance Registry System: 4-Piperidinemethanol, 1-benzoyl-(19980-00-8)

Safety Data

• Hazardous Substances Data: 19980-00-8(Hazardous Substances Data)

Upstream product

• 5274-99-7 1-benzoylisonipecotic acid 
• 543-27-1 isobutyl chloroformate 
• 2971-79-1 isonipecotic acid methyl ester 
• 98-88-4 benzoyl chloride 
• 6457-49-4 4-piperidinemethanol 
• 1126-09-6 4-carbethoxypiperidine 
• 17037-68-2 (4-methylpiperidin-1-yl)(phenyl)methanone 
• 613-90-1 benzoyl cyanide 
• 136081-74-8 ethyl 1-benzoyl-4-piperidine-carboxylate 

Downstream Products

• 184921-12-8 1-benzoyl-piperidin-4-ylmethyl methanesulfonate 
• 120014-29-1 1-benzoyl-piperidine-4-carboxaldehyde 
• 916976-35-7 (4-benzhydrylidene-piperidin-1-yl)-phenyl-methanone 
• 109555-51-3 1-benzoyl-4-benzoylpiperidine 
• 109932-47-0 (4-(hydroxy(phenyl)methyl)piperidin-1-yl)(phenyl)methanone 
• 149874-90-8 1-benzoyl-4-<(5,6-dimethoxy-1-oxoindan-2-ylidenyl)methyl>piperidine 
• 351532-13-3 2-[1-(3-iodo-benzyl)-piperidin-4-ylmethyl]-5,6-dimethoxy-indan-1-one 
• 313502-54-4 (+)-trans-1-hydroxymethyl-4-oxo-2-phenylcyclopentane 
• 63608-15-1 (4-(chloromethyl)piperidin-1-yl)(phenyl)methanone 
• 67686-01-5 1-benzyl-4-piperidinemethanol 
• 120013-38-9 2-((1-benzoylpiperidin-4-yl)methyl)-5,6-dimethoxy-2,3-dihydro-1H-inden-1-one 

Relevant articles and documents

A Bond-Weakening Borinate Catalyst that Improves the Scope of the Photoredox α-C-H Alkylation of Alcohols

The development of catalyst-controlled, site-selective C(sp 3)-H functionalization reactions is currently a major challenge in organic synthesis. In this paper, a novel bond-weakening catalyst that recognizes the hydroxy group of alcohols through formation of a borate is described. An electron-deficient borinic acid-ethanolamine complex enhances the chemical yield of the α-C-H alkylation of alcohols when used in conjunction with a photoredox catalyst and a hydrogen atom transfer catalyst under irradiation with visible light. This ternary hybrid catalyst system can, for example, be applied to functional-group-enriched-peptides.

cGAS ANTAGONIST COMPOUNDS

Disclosed are novel compounds of Formula (I) that are cGAS antagonists, methods of preparation of the compounds, pharmaceutical compositions comprising the compounds, and their use in medical therapy.

Highly chemoselective metal-free reduction of tertiary amides

This communication describes the chemoselective metal-free reduction of tertiary amides to the corresponding amines. Hantzsch ester is used as a mild reducing agent for the reduction of trifluoromethanesulfonic anhydride activated amides providing the tertiary amines with high functional group tolerance. Copyright