3-(N-Boc-amino)-1-propanesulfonic acid

Base Information

Chemical Name:3-(N-Boc-amino)-1-propanesulfonic acid
CAS No.:918825-10-2
Molecular Formula:C₈H₁₇NO₅S
Molecular Weight:239.293
Hs Code.:
DSSTox Substance ID:DTXSID10473584
Wikidata:Q82303080
Mol file:918825-10-2.mol

Synonyms:3-(N-Boc-amino)-1-propanesulfonic acid;918825-10-2;3-[(2-methylpropan-2-yl)oxycarbonylamino]propane-1-sulfonic Acid;3-((tert-Butoxycarbonyl)amino)propane-1-sulfonic acid;AB2681;SCHEMBL917886;DTXSID10473584;MFCD09037856;AKOS027339508;AS-44649;EN300-7424249;3-((tert-Butoxycarbonyl)amino)propane-1-sulfonicacid;3-{[(tert-butoxy)carbonyl]amino}propane-1-sulfonic acid

Suppliers and Price of 3-(N-Boc-amino)-1-propanesulfonic acid

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
3-(N-Boc-amino)-1-propanesulfonicAcid
500mg
$ 175.00

TRC
3-(N-Boc-amino)-1-propanesulfonicAcid
100mg
$ 60.00

Crysdot
3-((tert-Butoxycarbonyl)amino)propane-1-sulfonicacid 97%
5g
$ 391.00

Crysdot
3-((tert-Butoxycarbonyl)amino)propane-1-sulfonicacid 97%
10g
$ 587.00

American Custom Chemicals Corporation
3-(N-BOC-AMINO)-1-PROPANESULFONIC ACID 95.00%
5MG
$ 498.29

Total 2 raw suppliers

Chemical Property of 3-(N-Boc-amino)-1-propanesulfonic acid

Chemical Property:

PSA：101.08000
LogP:2.26070
XLogP3:0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:239.08274382
Heavy Atom Count:15
Complexity:298

Purity/Quality:

99% ^*data from raw suppliers

3-(N-Boc-amino)-1-propanesulfonicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCCCS(=O)(=O)O

Technology Process of 3-(N-Boc-amino)-1-propanesulfonic acid

There total 2 articles about 3-(N-Boc-amino)-1-propanesulfonic acid 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: