What is the 1,2,3,4-Tetrahydroquinoline?

1,2,3,4-Tetrahydroquinoline is clear pale yellow to yellow liquid, while it's Molecular Formula is C9H11N. clear pale yellow to yellow liquid 1,2,3,4-Tetrahydroquinoline is a reagent used in the synthesis of N-substituted benzoyl-1,2,3,4-tetrahydroquinolyl-1-carboxamides displaying fungicidal activity.

What is the CAS number for 1,2,3,4-Tetrahydroquinoline?

The CAS number of 1,2,3,4-Tetrahydroquinoline is 635-46-1.

What is 1,2,3,4-Tetrahydroquinoline (635-46-1) used for?

1,2,3,4-Tetrahydroquinoline is a heterocyclic organic compound with the chemical formula C9H11N. It is a derivative of quinoline, where four hydrogen atoms are added to the quinoline ring, resulting in a saturated structure. 1,2,3,4-Tetrahydroquinoline is known for its potential applications in various chemical and pharmaceutical processes due to its unique chemical properties.InChI:InChI=1/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6,10H,3,5,7H2

What is the 1,2,3,4-Tetrahydroquinoline?

1,2,3,4-Tetrahydroquinoline is clear pale yellow to yellow liquid, while it's Molecular Formula is C9H11N. clear pale yellow to yellow liquid 1,2,3,4-Tetrahydroquinoline is a reagent used in the synthesis of N-substituted benzoyl-1,2,3,4-tetrahydroquinolyl-1-carboxamides displaying fungicidal activity.

What is the CAS number for 1,2,3,4-Tetrahydroquinoline?

The CAS number of 1,2,3,4-Tetrahydroquinoline is 635-46-1.

What is 1,2,3,4-Tetrahydroquinoline (635-46-1) used for?

1,2,3,4-Tetrahydroquinoline is a heterocyclic organic compound with the chemical formula C9H11N. It is a derivative of quinoline, where four hydrogen atoms are added to the quinoline ring, resulting in a saturated structure. 1,2,3,4-Tetrahydroquinoline is known for its potential applications in various chemical and pharmaceutical processes due to its unique chemical properties.InChI:InChI=1/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6,10H,3,5,7H2

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635-46-1

Product Name：1,2,3,4-Tetrahydroquinoline
Molecular Formula：C₉H₁₁N
Purity：99%
Molecular Weight：133.193

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Product Details;

CasNo： 635-46-1

Molecular Formula： C₉H₁₁N

Appearance： clear pale yellow to yellow liquid

Quality Factory Supply 99% Pure 1,2,3,4-Tetrahydroquinoline 635-46-1 with Efficient Delivery

Molecular Formula:C9H11N
Molecular Weight:133.193
Appearance/Colour:clear pale yellow to yellow liquid
Vapor Pressure:0.0212mmHg at 25°C
Melting Point:9-14 °C(lit.)
Refractive Index:n20/D 1.593(lit.)
Boiling Point:250.775 °C at 760 mmHg
PKA:5.09±0.20(Predicted)
Flash Point:100.6 °C
PSA：12.03000
Density:1.006 g/cm³
LogP:2.18270

1,2,3,4-Tetrahydroquinoline(Cas 635-46-1) Usage

Synthesis Reference(s)	Chemical and Pharmaceutical Bulletin, 34, p. 3905, 1986 DOI: 10.1248/cpb.34.3905Tetrahedron, 52, p. 1631, 1996 DOI: 10.1016/0040-4020(95)00991-4
General Description	1,2,3,4-Tetrahydroquinoline is a bicyclic aromatic compound that serves as a substrate in enzymatic oxyfunctionalization reactions, yielding chiral synthons like (+)-(R)-1,2,3,4-tetrahydroquinoline-4-ol. It is also a key intermediate in hydrogenation processes, such as the selective reduction of quinoline using rhodium catalysts, and is utilized in the synthesis of heterocycles like epoxyisoindolo[2,1-a]quinolines and CETP inhibitors. Its derivatives exhibit potential pharmaceutical applications, including antihypoxic activity and modulation of lipid metabolism.
Definition	ChEBI: A member of the class of quinolines that is the 1,2,3,4-tetrahydro derivative of quinoline.

InChI:InChI=1/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6,10H,3,5,7H2

635-46-1 Relevant articles

Correction to: Halogen-Bonding-Induced Hydrogen Transfer to C=N Bond with Hantzsch Ester (Org. Lett. (2014) 16:12 (3244-3247) DOI: 10.1021/ol501259q)

He, Wei,Ge, Yi-Cen,Tan, Choon-Hong

, p. 7684 - 7684 (2019)

The structure of C1 has been revised in ...

Medium-Sized-Ring Analogues of Dibenzodiazepines by a Conformationally Induced Smiles Ring Expansion

Costil, Romain,Lefebvre, Quentin,Clayden, Jonathan

, p. 14602 - 14606 (2017)

Analogues of dibenzodiazepines, in which...

Study of Hydrodesulfurization by the Use of 35S-Labeled Dibenzothiophene. 2. Behavior of Sulfur in HDS, HDO, and HDN on Sulfided Mo/Al2O3 Catalyst

Kabe, Toshiaki,Quian, Weihua,Ishihara, Atsushi

, p. 912 - 916 (1994)

To investigate the behavior of sulfur du...

-

Tsodikov et al.

, (1967)

Ru-decorated N-doped carbon nanoflakes for selective hydrogenation of levulinic acid to γ-valerolactone and quinoline to tetrahydroquinoline with HCOOH in water

Chauhan, Arzoo,Kar, Ashish Kumar,Srivastava, Rajendra

, (2022/03/27)

The effective dissociation of biomass-de...

Dehydrogenative and Redox-Neutral N-Heterocyclization of Aminoalcohols Catalyzed by Manganese Pincer Complexes

Brzozowska, Aleksandra,Rueping, Magnus,Sklyaruk, Jan,Zubar, Viktoriia

, (2022/03/17)

A new manganese catalyzed heterocyclizat...

Chemoselective and Tandem Reduction of Arenes Using a Metal–Organic Framework-Supported Single-Site Cobalt Catalyst

Antil, Neha,Kumar, Ajay,Akhtar, Naved,Begum, Wahida,Chauhan, Manav,Newar, Rajashree,Rawat, Manhar Singh,Manna, Kuntal

supporting information, p. 1031 - 1040 (2022/01/19)

The development of heterogeneous, chemos...

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

-

Paragraph 0094-0095; 0114-0122, (2021/05/29)

The invention belongs to the technical f...

635-46-1 Process route

: 91-22-5
quinoline

: 10500-57-9
5,6,7,8-tetrahydroquinoline

: 635-46-1
1,2,3,4-tetrahydroisoquinoline

: 1678-92-8
propylcyclohexane

: 103-65-1
phenylpropane

: 1821-39-2
2-propylaniline

Conditions

Conditions	Yield
With hydrogen; ruthenium sulphide on HY-zeolite; In n-heptane; at 400 ℃; for 4.5h; under 25862.1 Torr; Product distribution; other catalysts;

: 50624-35-6
1,4-dihydroquinoline

: 1125-81-1
2-methyl-1,2-dihydroquinoline

: 635-46-1
1,2,3,4-tetrahydroisoquinoline

: 42307-21-1
2-Methyl-chinoliniumkation

: 1780-19-4
1,2,3,4-tetrahydro-2-methylquinoline