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51503-10-7

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51503-10-7 Usage

General Description

2-ISOPROPYLPYRROLIDINE is a chemical compound that belongs to the class of organic compounds known as pyrrolidines. It is a volatile, colorless liquid with a faint odor and is commonly used as a chemical intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a solvent and in the manufacturing of certain polymers. In addition, 2-ISOPROPYLPYRROLIDINE has been studied for its potential antiviral and antibacterial properties. Due to its versatility and wide range of applications, it is an important chemical compound in various industries. However, it is important to handle and use 2-ISOPROPYLPYRROLIDINE with caution as it can be harmful if ingested, inhaled, or comes into contact with the skin or eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 51503-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,0 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51503-10:
(7*5)+(6*1)+(5*5)+(4*0)+(3*3)+(2*1)+(1*0)=77
77 % 10 = 7
So 51503-10-7 is a valid CAS Registry Number.

51503-10-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-ylpyrrolidine

1.2 Other means of identification

Product number -
Other names 2-Isopropylpyrrolidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:51503-10-7 SDS

51503-10-7Downstream Products

51503-10-7Relevant articles and documents

A3-coupling reaction as a strategy towards the synthesis of alkaloids

Carmona, Rafaela C.,Wendler, Edison P.,Sakae, George H.,Comassetoa, Jo?o V.,Santos, Alcindo A. Dos

, p. 117 - 123 (2015/02/19)

A number of aldehydes, alkynols and benzylamines were submitted to A3-coupling reaction, under CuCl catalysis, giving strategically functionalized hydroxy-propargylamines. The procedure allows the use of alkyl as well as aryl aldehydes. Representative substrates were converted into five- and six-membered cyclic alkaloids by sequential one-pot N-debenzylation/triple bond reduction promoted by Pd, followed by a Mitsunobu-type cyclization.

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