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2,6-di-tert-butyl-4-(dimethylamino)-pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38222-90-1

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38222-90-1 Usage

Chemical compound

2,6-di-tert-butyl-4-(dimethylamino)-pyridine

Use

Catalyst in organic chemistry reactions

Properties

Strong base
Nucleophilic catalyst
Colorless, crystalline solid
Strong odor
Highly flammable
Relatively safe to handle

Applications

Acylation and alkylation reactions
Synthesis of esters, amides, and other organic compounds

Industries

Pharmaceutical industry
Fine chemical industry

Importance

Versatile organic synthesis reagent

Check Digit Verification of cas no

The CAS Registry Mumber 38222-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38222-90:
(7*3)+(6*8)+(5*2)+(4*2)+(3*2)+(2*9)+(1*0)=111
111 % 10 = 1
So 38222-90-1 is a valid CAS Registry Number.

38222-90-1SDS

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 2,6-ditert-butyl-N,N-dimethylpyridin-4-amine

1.2 Other means of identification

Product number -
Other names 2,6-di-tert-butyl-N,N-dimethylpyridin-4-amine

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:38222-90-1 SDS

38222-90-1Downstream Products

38222-90-1Relevant academic research and scientific papers

Peptide coupling in the presence of highly hindered tertiary amines

Carpino, Louis A.,Ionescu, Dumitru,El-Faham, Ayman

, p. 2460 - 2465 (1996)

Previously, 2,4,6-trimethylpyridine (collidine), due to steric shielding around the N-atom, was found to be an efficient base for effecting peptide segment coupling via azabenzotriazole-based onium-style coupling reagents. A number of even more highly hin

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