1,2,3,4-Tetrahydroquinoline, 98%

Name: 1,2,3,4-Tetrahydroquinoline, 98%
SKU: B22750.36
Price: 154.00 EUR

CAS: 635-46-1 | C9H11N | 133.19 g/mol

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Catalog number B22750.36

also known as B22750-36

Price (EUR)

154,00

Each

Quantity:

500 g

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Price (EUR)

154,00

Each

Chemical Identifiers

CAS635-46-1

IUPAC Name1,2,3,4-tetrahydroquinoline

Molecular FormulaC9H11N

InChI KeyLBUJPTNKIBCYBY-UHFFFAOYSA-N

SMILESC1CNC2=CC=CC=C2C1

Specifications

Specification Sheet

Appearance (Color)Clear pale yellow to yellow to brown

Assay (GC)≥97.5%

Refractive Index1.5930-1.5970 @ 20?C

Identification (FTIR)Conforms

FormLiquid

1,2,3,4-Tetrahydroquinoline is used as an antioxidant and corrosion inhibitor. It is an active component in various dyes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,2,3,4-Tetrahydroquinoline is used as an antioxidant and corrosion inhibitor. It is an active component in various dyes.

Solubility
Miscible with alcohol, ether, carbon disulfide and many organic solvents. Slightly miscible with water.

Notes
Hygroscopic. Incomaptible with strong oxidizing agents.

RUO – Research Use Only

General References:

2-Metallation can be effected in a one-pot sequence via the Li carbamate: J. Chem. Soc., Perkin 1, 17 (1989); cf Indole, A14427.
1,2,3,4-Tetrahydroquinoline derivatives are oxidized to N-hydroxy lactams by H₂O₂ in the presence of tungstate ion: J. Org. Chem., 55, 1744 (1990):
Liu, J.; Liu, F.; Zhu, Y.; Ma, X.; Jia, X. Oxidative Povarov Reaction via sp³ C-H Oxidation of N-Benzylanilines Induced by Catalytic Radical Cation Salt: Synthesis of 2,4-Diarylquinoline Derivatives. Org. Lett. 2015, 17 (6), 1409-1412.
Jiang, H. Y.; Zheng, X. X. Phosphine-functionalized ionic liquid-stabilized rhodium nanoparticles for selective hydrogenation of aromatic compounds. Appl. Catal., A 2015, 499, 118-123.