97475-96-2

Basic information

• Product Name: ethyl 1-Benzyl-1,4,5,6-Tetrahydrocyclopenta[b]Pyrrole-2-Carboxylate
• Synonyms: ethyl 1-Benzyl-1,4,5,6-Tetrahydrocyclopenta[b]Pyrrole-2-Carboxylate
• CAS NO: 97475-96-2
• Molecular Weight: 269.343
• Mol File: 97475-96-2.mol

Chemical Properties

• CAS DataBase Reference: ethyl 1-Benzyl-1,4,5,6-Tetrahydrocyclopenta[b]Pyrrole-2-Carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-Benzyl-1,4,5,6-Tetrahydrocyclopenta[b]Pyrrole-2-Carboxylate(97475-96-2)
• EPA Substance Registry System: ethyl 1-Benzyl-1,4,5,6-Tetrahydrocyclopenta[b]Pyrrole-2-Carboxylate(97475-96-2)

Safety Data

• Hazardous Substances Data: 97475-96-2(Hazardous Substances Data)

Upstream product

• 2611-03-2 2-chlorocyclopent-1-ene-1-carbaldehyde 
• 6436-90-4 ethyl 2-(benzylamino)acetate 
• 70-23-5 ethyl Bromopyruvate 
• 15814-19-4 N-cyclopentylidene-1-phenylmethanamine 
• 120-92-3 cyclopentanone 
• 100-46-9 benzylamine 

Downstream Products

• 164736-53-2 1-benzyl-1,4,5,6-tetrahydrocyclopentapyrrole-2-carboxylic acid 
• 87269-86-1 (1RS,3RS,5RS)-2-Azabicyclo<3.3.0>octan-3-carbonsaeure-hydrochlorid 
• 97475-97-3 ethyl octahydrocyclopenta[b]pyrrole-2-carboxylate 

Relevant articles and documents

Flow microwave technology and microreactors in synthesis

A bespoke microwave reactor with a glass containment cell has been developed for performing continuous flow reactions under microwave heating. The prototype unit has been evaluated using a series of standard organic chemical transformations enabling scale-up of these chemical processes. As part of the development, a carbon-doped PTFE reactor insert was utilized to allow the heating of poorly absorbing reaction media, increasing the range of solvents and scope of reactions that can be performed in the device.

Cis,endo-2-azabicycloalkane-3-carboxylic acid derivatives, their use and intermediates in their preparation

The invention relates to compounds of the formula I STR1 in which n is 1, 2 or 3, Z1 and Z2, and Z3 and Z4, in each case together represent a chemical bond or Z1, Z2, Z3 and Zsu

Angiotensin-converting enzyme inhibitors

Novel compounds with angiotensin-converting enzyme inhibitory activity are disclosed. Such compounds are useful in the treatment of cardiovascular disorders, especially hypertension and congestive heart failure, and are useful in the treatment of glaucoma

EINE EINFACHE DIASTEREOSELEKTIVE SYNTHESE VON (1SR,3SR,5SR)-2-AZABICYCLOOCTAN-3-CARBONSAEURE

(1SR,3SR,5SR)-2-Azabicyclooctane-3-carboxylic acid, precursor of the angiotensin-converting-enzyme-inhibitor Hoe 498, is easily prepared from 1-chloro-1-cyclopentene-2-carbaldehyde in three steps.