7335-07-1

Basic information

• Product Name: Pyrrolidine, 1-propyl-
• CAS NO: 7335-07-1
• Molecular Formula: C7H15N
• Molecular Weight: 113.203
• Mol File: 7335-07-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Pyrrolidine, 1-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrrolidine, 1-propyl-(7335-07-1)
• EPA Substance Registry System: Pyrrolidine, 1-propyl-(7335-07-1)

Safety Data

• Hazardous Substances Data: 7335-07-1(Hazardous Substances Data)

Usage

General Description

Pyrrolidine, 1-propyl- is a chemical compound with the formula C8H17N. It is an organic compound that belongs to the class of heterocyclic compounds, specifically those containing a pyrrolidine ring with a propyl substituent. It is a clear, colorless liquid with a slightly ammonia-like odor. Pyrrolidine, 1-propyl- has uses in a variety of industrial applications, including as a solvent and as a precursor to the synthesis of other organic compounds. It is also used in the manufacturing of pharmaceuticals and in organic synthesis processes. Additionally, it is used in the production of insecticides and agricultural chemicals. Despite its wide range of uses, exposure to high levels of pyrrolidine, 1-propyl- can be harmful, causing irritation to the skin, eyes, and respiratory system. As a result, it should be handled and stored with caution and in accordance with safety guidelines.

Upstream product

• 108-94-1 cyclohexanone 
• 135623-98-2 1-(1-Phenylsulfanyl-propyl)-pyrrolidine 
• 110-63-4 Butane-1,4-diol 

Downstream Products

• 607-68-1 2,4-dichloroquinazoline 
• 81683-45-6 4-chloro-2-(N-propyl-4-chlorobutylamino)quinazoline 
• 19748-66-4 3-pyrrolidin-1-yl-propan-1-ol 
• 42122-41-8 1‐(pyrrolidin‐1‐yl)propan‐2‐ol 
• 10220-22-1 1-(4-nitro-phenyl)-pyrrolidine 

Relevant articles and documents

One-pot synthesis of 1-butylpyrrolidine and its derivatives from aqueous ammonia and 1,4-butandiol over CuNiPd/ZSM-5 catalysts

The synthesis of 1-butylpyrrolidine and its derivatives (1-butylpyrrolidine with a little of 1-butenylpyrrolidines) was developed via a one-pot method from ammonia and 1,4-butandiol. Here, the product of 1-butylpyrrolidine was emphatically investigated, and the yield was 76% under the optimized conditions. Such a route was realized through successive N-alkylation using aqueous ammonia as the nitrogen source over the CuNiPd/ZSM-5 catalyst, which was prepared by a simple incipient wetness method. In this route, 1,4-butandiol not only participated in the formation of the N-heterocycle, but also acted as an alkylating reagent. This work offers a straightforward, economical route for 1-butylpyrrolidine and its derivatives. This journal is

SITE-SPECIFIC GENERATION OF NONSTABILIZED α-AMINOCARBANIONS. A NOVEL METHODOLOGY TOWARD THE SYNTHESIS OF 2-AMINOALCOHOLS

A method for site-specific generation of "nonstabilized" α-aminocarbanions with no activating or stabilizing group was developed, utilizing a metal-sulfur exchange reaction.The method provides a novel methodology for the synthesis of 2-aminoalcohols.