2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one

Base Information

Chemical Name:2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one
CAS No.:133886-43-8
Molecular Formula:C14H15NO3S
Molecular Weight:277.344
Hs Code.:2933990090
DSSTox Substance ID:DTXSID90431642
Nikkaji Number:J729.051I
Mol file:133886-43-8.mol

Synonyms:2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one;133886-43-8;2-(4-methylphenyl)sulfonyl-1,3,6,6a-tetrahydrocyclopenta[c]pyrrol-5-one;SCHEMBL6771459;DTXSID90431642;AKOS004902836;3-Tosyl-3-azabicyclo[3.3.0]octa-5-ene-7-one;2,3,3a,4-Tetrahydro-2-[(4-methylphenyl)sulfonyl]-cyclopenta[c]pyrrol-5(1H)-one

Suppliers and Price of 2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one

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

Crysdot
2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one 95+%
1g
$ 772.00

Chemenu
2-tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one 95%
1g
$ 729.00

American Custom Chemicals Corporation
2-TOSYL-2,3,3A,4-TETRAHYDROCYCLOPENTA[C]PYRROL-5(1H)-ONE 95.00%
5MG
$ 498.10

Total 5 raw suppliers

Chemical Property of 2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one

Chemical Property:

PSA：62.83000
LogP:2.53340
XLogP3:0.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:277.07726451
Heavy Atom Count:19
Complexity:509

Purity/Quality:

99% ^*data from raw suppliers

2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N2CC3CC(=O)C=C3C2

Technology Process of 2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one

There total 21 articles about 2-Tosyl-2,3,3a,4-tetrahydrocyclopenta[c]pyrrol-5(1H)-one 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: 98.0%

: 201230-82-2
carbon monoxide

: 133886-40-5
N-tosyl-N-allylpropargylamine

: 133886-43-8
2,3,3a,4-tetrahydro-2-[(4-methylphenyl)sulfonyl]-cyclopenta[c]pyrrol-5(1H)-one

Guidance literature:: Co/C; In tetrahydrofuran; at 130 ℃; for 7h; under 15200 Torr;

Reference yield: 97.0%

: 15226-74-1,61091-28-9,61117-58-6
dicobalt octacarbonyl

: 133886-40-5
N-tosyl-N-allylpropargylamine

: 133886-43-8
2,3,3a,4-tetrahydro-2-[(4-methylphenyl)sulfonyl]-cyclopenta[c]pyrrol-5(1H)-one

Guidance literature:: dicobalt octacarbonyl; N-tosyl-N-allylpropargylamine; In dichloromethane; at 20 ℃; for 0.5h;

With 4-methylmorpholine N-oxide; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jo8017439

Reference yield: 95.0%

: 133886-40-5
N-tosyl-N-allylpropargylamine

: 133886-43-8
2,3,3a,4-tetrahydro-2-[(4-methylphenyl)sulfonyl]-cyclopenta[c]pyrrol-5(1H)-one

Guidance literature:: N-tosyl-N-allylpropargylamine; Co₂(CO)8; In dichloromethane;

With N-methyl-2-indolinone; In dichloromethane; at 25 ℃; for 16h;
DOI:10.1016/S0040-4039(02)01912-3