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383127-39-7

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383127-39-7 Usage

General Description

2-(2,6-dichlorophenyl)pyrrolidine is a chemical compound with the molecular formula C10H11Cl2N. It is a white to light brown solid that is soluble in organic solvents. 2-(2,6-dichlorophenyl)pyrrolidine is used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has potential applications as an intermediate in the production of insecticides and other biologically active compounds. Additionally, research has shown that 2-(2,6-dichlorophenyl)pyrrolidine may have neuroprotective and anti-inflammatory properties, making it a potentially valuable compound for the development of new medicinal products. However, it is important to handle this compound with caution, as it may be harmful if ingested or inhaled and can cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 383127-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,2 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 383127-39:
(8*3)+(7*8)+(6*3)+(5*1)+(4*2)+(3*7)+(2*3)+(1*9)=147
147 % 10 = 7
So 383127-39-7 is a valid CAS Registry Number.

383127-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-DICHLOROPHENYL)PYRROLIDINE

1.2 Other means of identification

Product number -
Other names -

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:383127-39-7 SDS

383127-39-7Downstream Products

383127-39-7Relevant articles and documents

α-Functionalization of Cyclic Secondary Amines: Lewis Acid Promoted Addition of Organometallics to Transient Imines

Paul, Anirudra,Seidel, Daniel

, p. 8778 - 8782 (2019)

Cyclic imines, generated in situ from their corresponding N-lithiated amines and a ketone hydride acceptor, undergo reactions with a range of organometallic nucleophiles to generate α-functionalized amines in a single operation. Activation of the transient imines by Lewis acids that are compatible with the presence of lithium alkoxides was found to be crucial to accommodate a broad range of nucleophiles including lithium acetylides, Grignard reagents, and aryllithiums with attenuated reactivities.

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