7335-07-1 Usage
Description
Pyrrolidine, 1-propyl-, also known as 1-Propylpyrrolidine, is a heterocyclic organic compound with the chemical formula C8H17N. It features a pyrrolidine ring with a propyl substituent, giving it a clear, colorless liquid appearance and a slightly ammonia-like odor. Pyrrolidine, 1-propylis utilized in various industrial applications, such as a solvent, precursor in the synthesis of other organic compounds, and in the production of pharmaceuticals, insecticides, and agricultural chemicals.
Uses
Used in Chemical Synthesis Industry:
Pyrrolidine, 1-propylis used as a precursor in the synthesis of other organic compounds, contributing to the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Pyrrolidine, 1-propylserves as a crucial component in the manufacturing process of various medications, playing a significant role in the development of new drugs.
Used in Agriculture:
Pyrrolidine, 1-propylis utilized in the production of insecticides and agricultural chemicals, helping to protect crops and enhance agricultural productivity.
Used as a Solvent:
Pyrrolidine, 1-propylalso functions as a solvent in different industrial processes, aiding in the dissolution and handling of various substances.
Safety Precautions:
Despite its wide range of applications, exposure to high levels of Pyrrolidine, 1-propylcan be harmful, causing irritation to the skin, eyes, and respiratory system. Therefore, it should be handled and stored with caution, adhering to safety guidelines to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 7335-07-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7335-07:
(6*7)+(5*3)+(4*3)+(3*5)+(2*0)+(1*7)=91
91 % 10 = 1
So 7335-07-1 is a valid CAS Registry Number.
7335-07-1Relevant articles and documents
One-pot synthesis of 1-butylpyrrolidine and its derivatives from aqueous ammonia and 1,4-butandiol over CuNiPd/ZSM-5 catalysts
Long, Yan,Liu, Shimin,Ma, Xiangyuan,Lu, Liujin,He, Yude,Deng, Youquan
supporting information, p. 16708 - 16712 (2020/10/27)
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
Tsunoda, Tetsuto,Fujiwara, Kenshu,Yamamoto, Yo-ichi,Ito, Sho
, p. 1975 - 1978 (2007/10/02)
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.