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(3AR,7aR)-octahydro-1H-indole

Base Information
  • Chemical Name:(3AR,7aR)-octahydro-1H-indole
  • CAS No.:1193-68-6
  • Molecular Formula:C8H15N
  • Molecular Weight:125.214
  • Hs Code.:
  • European Community (EC) Number:889-828-9
  • Mol file:1193-68-6.mol
(3AR,7aR)-octahydro-1H-indole

Synonyms:(3AR,7aR)-octahydro-1H-indole;752169-56-5;1193-68-6;(3AR,7AR)-REL-OCTAHYDRO-1H-INDOLE (RELATIVE STRUC);SCHEMBL4450273;AKOS026741573;1H-Indole,octahydro-,(3ar-cis)-(9ci);EN300-197562;(3aR,7aR)-2,3,3a,4,5,6,7,7a-octahydro-1H-indole;Z1203749443

Suppliers and Price of (3AR,7aR)-octahydro-1H-indole
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (3ar,7ar)-Octahydro-1H-indole
  • 250mg
  • $ 310.00
  • TRC
  • (3ar,7ar)-Octahydro-1H-indole
  • 50mg
  • $ 90.00
  • AccelPharmtech
  • (3aR,7aR)-rel-octahydro-1H-Indole(Relativestruc) 97.00%
  • 25G
  • $ 4010.00
  • AccelPharmtech
  • (3aR,7aR)-rel-octahydro-1H-Indole(Relativestruc) 97.00%
  • 5G
  • $ 2180.00
  • AccelPharmtech
  • (3aR,7aR)-rel-octahydro-1H-Indole(Relativestruc) 97.00%
  • 1G
  • $ 1940.00
Total 5 raw suppliers
Chemical Property of (3AR,7aR)-octahydro-1H-indole
Chemical Property:
  • PSA:12.03000 
  • LogP:1.86730 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:125.120449483
  • Heavy Atom Count:9
  • Complexity:101
Purity/Quality:

99% *data from raw suppliers

(3ar,7ar)-Octahydro-1H-indole *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC2C(C1)CCN2
  • Isomeric SMILES:C1CC[C@@H]2[C@H](C1)CCN2
Technology Process of (3AR,7aR)-octahydro-1H-indole

There total 22 articles about (3AR,7aR)-octahydro-1H-indole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 5%-palladium/activated carbon; hydrogen; In 2,2,2-trifluoroethanol; at 50 ℃; for 8h; under 5250.53 Torr;
DOI:10.1039/c2ob25980j
Guidance literature:
With 1,4-dioxane; nickel; at 220 ℃; under 183877 - 220652 Torr; Hydrogenation;
DOI:10.1021/ja01851a020
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