7037-44-7

Basic information

• Product Name: Benzeneacetyl chloride, a-cyclopentyl-
• CAS NO: 7037-44-7
• Molecular Formula: C13H15ClO
• Molecular Weight: 222.715
• Mol File: 7037-44-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzeneacetyl chloride, a-cyclopentyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetyl chloride, a-cyclopentyl-(7037-44-7)
• EPA Substance Registry System: Benzeneacetyl chloride, a-cyclopentyl-(7037-44-7)

Safety Data

• Hazardous Substances Data: 7037-44-7(Hazardous Substances Data)

Downstream Products

• 1094467-25-0 C₄₈H₆₈N₄O₂₁ 
• 175343-28-9 2-cyclopentyl-2-phenylethan-1-amine 
• 3900-94-5 cyclopentyl-phenyl-acetic acid amide 
• 58007-86-6 C₂₄H₃₀ 
• 133658-87-4 (Z)-1-cyclopentyl-1-phenyl-2-trimethylsilyloxy-1-hexene 
• 133658-84-1 {1-[1-Cyclopentyl-1-phenyl-meth-(E)-ylidene]-pentyloxy}-trimethyl-silane 
• 133658-93-2 (E)-1-cyclopentyl-3,3-dimethyl-1-phenyl-2-trimethylsilyloxy-1-butene 
• 133658-90-9 {1-[1-Cyclopentyl-1-phenyl-meth-(Z)-ylidene]-2,2-dimethyl-propoxy}-trimethyl-silane 
• 73363-20-9 1-<(Cyclopentylphenylacetoxy)ethyl>quinuclidinium bromide 
• 73330-90-2 1-(2-Hydroxyethyl)pyrrolizidinium bromide α-phenylcyclopentaneacetate 
• 437762-20-4 ethoxycarbonylmethylnortropyl N_α-phenylcyclopentylacetate 
• 437762-19-1 methoxycarbonylmethylnortropyl N_α-phenylcyclopentylacetate 
• 437762-21-5 (1R,3R,5S)-3-(2-Cyclopentyl-2-phenyl-acetoxy)-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid 1-chloro-ethyl ester 

Relevant articles and documents

Soft drugs: III. A new class of anticholinergic agents

A new class of antimuscarinic drugs was designed and synthesized. The compounds are 'soft' quaternary ammonium esters in which there is only one carbon atom separating the ester oxygen and the quaternary head. The compounds are potent anticholinergics when derived from hindered 'umbrella' acids and cholinergics when derivatives of simple aliphatic acids. The more potent anticholinergics have up to 10 times higher acetylcholine antagonist activity than atropine, but they have a much shorter duration of action. The compounds cleave hydrolytically with simultaneous destruction of the quaternary head. The compounds are promising as selective, local agents, particularly as inhibitors of eccrine sweating.