6-Chloro-1,2,3,4-Tetrahydroquinoline

• CAS: 49716-18-9
• Catalog Number: ACM49716189
• Category: Other Products
• Molecular Weight: 167.64
• Molecular Formula: C9H10NCl
• Synonyms: 6-chloro-1,2,3,4-tetrahydroquinoline, 49716-18-9, 6-chloro-1,2,3,4-tetrahydro-quinoline, chlorotetrahydroquinoline, ACMC-209khr, AC1Q3KLJ, SureCN1091532, CTK1D0536, MolPort-004-306-168, ANW-30829, ZINC12946161, AKOS000143150, AG-L-60208, AG-L-64303, MB06841, MCULE-3415212833, RP10415, SS-4320, Quinoline, 6-chloro-;6-chloroquinline;, AK-43157
• IUPAC Name: 6-chloro-1,2,3,4-tetrahydroquinoline
• Canonical SMILES: C1CC2=C(C=CC(=C2)Cl)NC1
• InChI Key: PASUADIMFGAUDB-UHFFFAOYSA-N
• Boiling Point: 288.1ºC at 760 mmHg
• Flash Point: 128ºC
• Density: 1.162g/cm³
• Exact Mass: 167.05000
• H-Bond Acceptor: 1
• H-Bond Donor: 1

Synthetic Use

Upstream Synthesis Route 1

• 612-57-7

• 49716-18-9

Reference: [1] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 17, p. 7956 - 7967

Upstream Synthesis Route 2

• 612-57-7

• 635-46-1
• 49716-18-9

Reference: [1] Journal of the American Chemical Society, 2012, vol. 134, # 42, p. 17592 - 17598,7
[2] Molecular Catalysis, 2018, vol. 452, p. 145 - 153

Upstream Synthesis Route 3

• 612-57-7

• 635-46-1
• 49716-18-9
• 767-92-0

Reference: [1] ACS Catalysis, 2016, vol. 6, # 9, p. 5816 - 5822

Upstream Synthesis Route 4

• 612-57-7

• 49716-18-9

Reference: [1]Bioorganic and Medicinal Chemistry,2008,vol. 16,p. 7956 - 7967

Upstream Synthesis Route 5

• 4169-19-1

• 49716-18-9

Reference: [1]Journal of the American Chemical Society,1952,vol. 74,p. 3176
[2]Chemical and Pharmaceutical Bulletin,1980,vol. 28,p. 3639 - 3648