1,4-Diazaspiro[4.5]decan-2-one

Base Information

Chemical Name:1,4-Diazaspiro[4.5]decan-2-one
CAS No.:19718-88-8
Molecular Formula:C₈H₁₄N₂O
Molecular Weight:154.212
Hs Code.:2933998090
DSSTox Substance ID:DTXSID30519837
Nikkaji Number:J2.812.443K
Wikidata:Q82383313
Mol file:19718-88-8.mol

Synonyms:1,4-diazaspiro[4.5]decan-2-one;19718-88-8;1,4-diazaspiro[4.5]decan-3-one;SCHEMBL8029442;DTXSID30519837;FLZYHGIIDJMSJQ-UHFFFAOYSA-N;1,4-diazaspiro[4,5]decan-2-one;MFCD14584836;AKOS005071638;AE-0754;CS-0199355;E78017;J-503977

Suppliers and Price of 1,4-Diazaspiro[4.5]decan-2-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

Matrix Scientific
1,4-Diazaspiro[4.5]decan-2-one >95%
500mg
$ 362.00

Crysdot
1,4-Diazaspiro[4.5]decan-2-one 95+%
1g
$ 427.00

Chemenu
1,4-Diazaspiro[4.5]decan-2-one 95%
1g
$ 403.00

American Custom Chemicals Corporation
1,4-DIAZASPIRO[4.5]DECAN-2-ONE 95.00%
500MG
$ 791.52

Ambeed
1,4-Diazaspiro[4.5]decan-2-one 95+%
250mg
$ 165.00

Ambeed
1,4-Diazaspiro[4.5]decan-2-one 95+%
100mg
$ 105.00

Ambeed
1,4-Diazaspiro[4.5]decan-2-one 95+%
1g
$ 435.00

Alichem
1,4-Diazaspiro[4.5]decan-2-one
1g
$ 448.24

AK Scientific
1,4-Diazaspiro[4.5]decan-2-one
500mg
$ 538.00

Total 9 raw suppliers

Chemical Property of 1,4-Diazaspiro[4.5]decan-2-one

Chemical Property:

PSA：41.13000
LogP:1.02380
XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:154.110613074
Heavy Atom Count:11
Complexity:173

Purity/Quality:

98%min ^*data from raw suppliers

1,4-Diazaspiro[4.5]decan-2-one >95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC2(CC1)NCC(=O)N2
General Description 1,4-Diazaspiro[4.5]decan-2-one is a spirocyclic compound that serves as a key intermediate in the synthesis of aminoquinoline derivatives via electrophilic rearrangement with Vilsmeier-Haack reagent, as well as in the environmentally friendly preparation of quinazolinones under mild, catalyst-free conditions. Its reactivity enables efficient transformations into structurally diverse heterocycles, including spiropiperidinequinazolinones, with high yields.

Technology Process of 1,4-Diazaspiro[4.5]decan-2-one

There total 5 articles about 1,4-Diazaspiro[4.5]decan-2-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: 96.0%