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22120-50-9

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22120-50-9 Usage

Description

2,3-DIMETHYLINDOLINE is a colorless to light yellow liquid heterocyclic compound with a bicyclic structure, featuring both a benzene ring and a five-membered nitrogen-containing ring. It is primarily utilized as a reactive intermediate in the synthesis of various organic compounds, including pharmaceuticals, dyes, and other organic materials. Known for its potential as a corrosion inhibitor and a photochemical precursor for polymer production, 2,3-DIMETHYLINDOLINE is recognized for its low toxicity and minimal adverse effects on human health or the environment when handled with standard safety measures.

Uses

Used in Pharmaceutical Industry:
2,3-DIMETHYLINDOLINE serves as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds. Its unique structure allows for versatile chemical reactions, facilitating the creation of a wide range of therapeutic agents.
Used in Dye Industry:
As a reactive intermediate, 2,3-DIMETHYLINDOLINE is used in the production of dyes, enabling the synthesis of various colorants for different applications, including textiles, plastics, and printing inks.
Used in Corrosion Inhibition:
2,3-DIMETHYLINDOLINE exhibits potential as a corrosion inhibitor, protecting metal surfaces from degradation and extending the service life of materials in various industrial applications.
Used in Polymer Production:
2,3-DIMETHYLINDOLINE acts as a photochemical precursor in the production of polymers, contributing to the development of new polymeric materials with specific properties for diverse uses in industries such as plastics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 22120-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,2 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22120-50:
(7*2)+(6*2)+(5*1)+(4*2)+(3*0)+(2*5)+(1*0)=49
49 % 10 = 9
So 22120-50-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N/c1-7-8(2)11-10-6-4-3-5-9(7)10/h3-8,11H,1-2H3

22120-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-DIMETHYLINDOLINE

1.2 Other means of identification

Product number -
Other names 1,2-dimethylindoline

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:22120-50-9 SDS

22120-50-9Relevant articles and documents

Kinetic Resolution of 2-Substituted Indolines by N-Sulfonylation using an Atropisomeric 4-DMAP-N-oxide Organocatalyst

Murray, James I.,Flodén, Nils J.,Bauer, Adriano,Fessner, Nico D.,Dunklemann, Daniel L.,Bob-Egbe, Opetoritse,Rzepa, Henry S.,Bürgi, Thomas,Richardson, Jeffery,Spivey, Alan C.

supporting information, p. 5760 - 5764 (2017/05/12)

The first catalytic kinetic resolution by N-sulfonylation is described. 2-Substituted indolines are resolved (s=2.6–19) using an atropisomeric 4-dimethylaminopyridine-N-oxide (4-DMAP-N-oxide) organocatalyst. Use of 2-isopropyl-4-nitrophenylsulfonyl chloride is critical to the stereodiscrimination and enables facile deprotection of the sulfonamide products with thioglycolic acid. A qualitative model that accounts for the stereodiscrimination is proposed.

Deoxygenation Reactions of ortho-Nitrostyrenes with Carbon Monoxide Catalysed by Metal Carbonyls: a New Route to Indoles

Crotti, Corrado,Cenini, Sergio,Rindone, Bruno,Tollari, Stefano,Demartin, Francesco

, p. 784 - 786 (2007/10/02)

The metal carbonyls Fe(CO)5, Ru3(CO)12, and Rh6(CO)16 are catalysts for the deoxygenation of ortho-nitrostyrenes under carbon monoxide pressure to give indole derivatives; the crystal structure of a non-catalytically active rhodium complex obtained during the synthesis of (5e) is reported.

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