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2,3-Lutidine

Catalog Number
ACM583619
Product Name
2,3-Lutidine
Structure
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CAS
583-61-9
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Synonyms
2,3-Dimethylpyridine; Pyridine, 2,3-dimethyl-
IUPAC Name
2,3-dimethylpyridine
Molecular Weight
107.15
Molecular Formula
C7H9N
Canonical SMILES
CC1=C(N=CC=C1)C
InChI
HPYNZHMRTTWQTB-UHFFFAOYSA-N
InChI Key
InChI=1S/C7H9N/c1-6-4-3-5-8-7(6)2/h3-5H,1-2H3
Boiling Point
162-163 °C -lit.
Melting Point
-15 °C -lit.
Purity
98%+
Appearance
Colorless liquid
Storage
Flammables area
Complexity
70.8
Covalently-Bonded Unit Count
1
EC Number
248-287-3; 209-514-1
Exact Mass
107.073499291
H-Bond Acceptor
1
Heavy Atom Count
8
Monoisotopic Mass
107.073499291
NSC Number
2157
Rotatable Bond Count
0
Topological Polar Surface Area
12.9 Ų
UNII
5Q0F649H6G
Vapor Pressure
2.69 mmHg;
Application
2,3-Lutidine, a derivative of pyridine, is a versatile and commercially available organic reagent widely utilized in various industries. Its primary purpose is to serve as an intermediate in organic synthesis, offering significant utility in the development of complex compounds. Additionally, 2,3-Lutidine functions as an acid-binding agent, enhancing chemical reactions by stabilizing acidic environments. In the pharmaceutical industry, it plays a crucial role as an intermediate in the synthesis of lansoprazole, an important medication. Beyond pharmaceuticals, it also finds use as a flavoring additive in the food industry, contributing subtle nuances to food products. This clear, colorless to slightly yellow liquid is an indispensable component in both scientific and industrial applications, facilitating innovation and function across diverse fields.
December 04, 2024

Essential Reagent for Organic Synthesis

We used Alfa Chemistry's 2,3-Lutidine in our lab, primarily as an acid-binding agent. Its purity and performance significantly enhanced our synthesis processes. This versatile reagent is now a staple in our research.

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