CAS 833453-93-3 | Quinoline, 1,2,3,4-tetrahydro-1-methyl-2-pentyl-, (2S)- | CAS Number 833453-93-3

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833453-93-3 | Quinoline, 1,2,3,4-tetrahydro-1-methyl-2-pentyl-, (2S)-

CAS No: 833453-93-3 Catalog No: AG0055SK MDL No:

Product Description

Catalog Number:

AG0055SK

Chemical Name:

Quinoline, 1,2,3,4-tetrahydro-1-methyl-2-pentyl-, (2S)-

CAS Number:

833453-93-3

Molecular Formula:

C15H23N

Molecular Weight:

217.3498

IUPAC Name:

(2S)-1-methyl-2-pentyl-3,4-dihydro-2H-quinoline

InChI:

InChI=1S/C15H23N/c1-3-4-5-9-14-12-11-13-8-6-7-10-15(13)16(14)2/h6-8,10,14H,3-5,9,11-12H2,1-2H3/t14-/m0/s1

InChI Key:

KSQZVAWGIAAZHJ-AWEZNQCLSA-N

SMILES:

CCCCC[C@H]1CCc2c(N1C)cccc2

Properties

Complexity:

202

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

217.183g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

217.356g/mol

Monoisotopic Mass:

217.183g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

3.2A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

4.8

Literature

Title	Journal
Conjugate addition of lithium N-phenyl-N-(α-methylbenzyl)amide: application to the asymmetric synthesis of (R)-(-)-angustureine.	Organic letters 20110520
Gold-catalyzed intramolecular allylic amination of 2-tosylaminophenylprop-1-en-3-ols. A concise synthesis of (+/-)-angustureine.	The Journal of organic chemistry 20090821
Organocatalytic approach to benzofused nitrogen-containing heterocycles: enantioselective total synthesis of (+)-angustureine.	Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
Antiplasmodial and cytotoxic activity of galipinine and other tetrahydroquinolines from Galipea officinalis.	Planta medica 20020101