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36075-06-6

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36075-06-6 Usage

General Description

2-Diethylaminopyridine is a chemical compound with the molecular formula C9H14N2. It is a tertiary amine that is commonly used as a catalyst in a variety of chemical reactions, including the acylation of alcohols, phenols, and amines, the esterification of carboxylic acids, and the urethane formation from isocyanates. 2-Diethylaminopyridine is often employed as a strong base due to its basic properties, and it is also used in the synthesis of pharmaceuticals, agrochemicals, and polymers. Additionally, it is known for its ability to facilitate reactions without the need for additional solvents or reagents, making it a versatile and valuable tool in the field of organic chemistry. While it has been shown to have low toxicity, proper precautions should still be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 36075-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,7 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36075-06:
(7*3)+(6*6)+(5*0)+(4*7)+(3*5)+(2*0)+(1*6)=106
106 % 10 = 6
So 36075-06-6 is a valid CAS Registry Number.

36075-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-DIETHYLAMINOPYRIDINE

1.2 Other means of identification

Product number -
Other names 2-Pyridinamine,N,N-diethyl

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:36075-06-6 SDS

36075-06-6Relevant articles and documents

Chemistry of heteroaryltriphenylphosphonium iodides: Preparation from iodoheteroaromatics and elimination of the phosphonium iodide group using basic solvents

Sato, Akihiro,Sugimoto, Osamu,Tanji, Ken-ichi

experimental part, p. 2735 - 2739 (2010/04/25)

α- and γ-Iodoheteroaromatics were found to react with triphenylphosphine to give heteroaromatictriphenylphosphonium iodides in excellent yields, β-lodoheteroaromatics, which are less reactive with triphenylphosphine compared to α- or γ-compounds, were con

BASE-INITIATED REACTIONS OF N-FLUOROPYRIDINIUM SALTS; A NOVEL CYCLIC CARBENE PROPOSED AS A REACTIVE SPECIES

Unemoto, Teruo,Tomizawa, Ginjiro

, p. 2705 - 2708 (2007/10/02)

A new type of base-initiated reactions of pyridinium salts was found and a novel cyclic carbene was proposed as the reactive species.

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