1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI)

Base Information

Chemical Name:1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI)
CAS No.:615268-29-6
Molecular Formula:C10H17N
Molecular Weight:151.25
Hs Code.:
Mol file:615268-29-6.mol

Synonyms:1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI)

Suppliers and Price of 1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI)

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of 1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI)

Chemical Property:

PSA：3.24000
LogP:1.98470

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI)

There total 4 articles about 1H-Pyrrolizine,hexahydro-1,1-dimethyl-2-methylene-,(7aS)-(9CI) 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:

: 477952-40-2
6-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-3-hydroxy-2-methyl-2-nitrohexane

: 615268-29-6
(7S)-1,1-dimethyl-2-methylenepyrrolizidine

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / oxalyl chloride; DMSO; triethylamine / CH₂Cl₂ / 1.33 h / cooling

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; 1: Swern oxidation;
DOI:10.1016/j.tet.2006.03.063

Reference yield:

: 477952-40-2
6-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-3-hydroxy-2-methyl-2-nitrohexane

: 615268-29-6
(7R)-1,1-dimethyl-2-methylenepyrrolizidine

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / oxalyl chloride; DMSO; triethylamine / CH₂Cl₂ / 1.33 h / cooling

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; 1: Swern oxidation;
DOI:10.1016/j.tet.2006.03.063