(3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine

Base Information

Chemical Name:(3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine
CAS No.:42607-24-9
Molecular Formula:C₁₃H₂₅N
Molecular Weight:195.348
Hs Code.:
DSSTox Substance ID:DTXSID201292670
Nikkaji Number:J2.373.463J

Synonyms:3-Butyloctahydro-5-methylindolizine;3-butyl-5-methylindolizidine;SCHEMBL11490696;HFUFMWLNHRIKMV-UHFFFAOYSA-N;DTXSID201292670;195B 3,5-Indolizidine (5Z,9Z);42607-24-9;(3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine

Suppliers and Price of (3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:195.198699802
Heavy Atom Count:14
Complexity:178

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCC1CCC2N1C(CCC2)C

Technology Process of (3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine

There total 1 articles about (3S,5R,8aR)-3-Butyl-5-methyloctahydroindolizine 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:

Reference yield:

: 21889-88-3
hept-6-en-2-one

: 78389-72-7
1-iodo-2-hexanone

: 42607-24-9,53447-41-9,53447-42-0,53447-43-1,53447-44-2,79465-32-0,82262-91-7,92841-44-6,94535-27-0,97371-88-5,97371-89-6,107597-44-4,118015-64-8,139345-64-5,150134-98-8
3-butyl-5-methyloctahydroindolizine

Guidance literature:: Multi-step reaction with 2 steps

1: di-tert-butoxydiazene; bis(tri-n-butyltin); pyridine-3-sulfonyl azide / benzene / 2.5 h / 70 °C / Inert atmosphere

2: hydrogenchloride; palladium on carbon; hydrogen / methanol; water / 96 h / 20 °C / 22502.3 Torr

With hydrogenchloride; di-tert-butoxydiazene; palladium on carbon; hydrogen; bis(tri-n-butyltin); pyridine-3-sulfonyl azide; In methanol; water; benzene;
DOI:10.1002/chem.201003137