Boc-Dab(Aloc)-OH

Base Information

Chemical Name:Boc-Dab(Aloc)-OH
CAS No.:171820-73-8
Molecular Formula:C13H22N2O6
Molecular Weight:302.32400
Hs Code.:
DSSTox Substance ID:DTXSID60427330
Wikidata:Q82239999
Mol file:171820-73-8.mol

Synonyms:Boc-Dab(Aloc)-OH;171820-73-8;(S)-4-(((Allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoic acid;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-(prop-2-enoxycarbonylamino)butanoic acid;Nalpha-Boc-Ngamma-allyloxycarbonyl-L-2,4-diaminobutyric acid;Na-Boc-Ng-allyloxycarbonyl-L-2,4-diaminobutyric acid;DTXSID60427330;AKOS015901094;CS-0267370;EN300-7364180;(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-{[(prop-2-en-1-yloxy)carbonyl]amino}butanoic acid;(S)-4-(((Allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoicacid

Suppliers and Price of Boc-Dab(Aloc)-OH

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
Boc-dab(aloc)-oh
25mg
$ 55.00

Crysdot
(S)-4-(((Allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoicacid 95+%
1g
$ 339.00

Chemenu
(S)-4-(((Allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)butanoicacid 95%
1g
$ 320.00

Total 11 raw suppliers

Chemical Property of Boc-Dab(Aloc)-OH

Chemical Property:

PSA：113.96000
LogP:2.04840
Storage Temp.:2-8°C
XLogP3:1.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:10
Exact Mass:302.14778643
Heavy Atom Count:21
Complexity:389

Purity/Quality:

99% ^*data from raw suppliers

Boc-dab(aloc)-oh ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CCNC(=O)OCC=C)C(=O)O
Isomeric SMILES:CC(C)(C)OC(=O)N[C@@H](CCNC(=O)OCC=C)C(=O)O

Technology Process of Boc-Dab(Aloc)-OH

There total 2 articles about Boc-Dab(Aloc)-OH 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:

: 25691-37-6,80445-78-9
(2S)-4-amino-2-[(tert-butoxycarbonyl)amino]butanoic acid

: 2937-50-0
Allyl chloroformate

: 171820-73-8
Boc-Dab(Alloc)-OH

Guidance literature:: With potassium carbonate; In diethyl ether; water; at 20 ℃;
DOI:10.1055/s-0036-1588393

Reference yield:

: 13726-85-7
Boc-Gln-OH

: 171820-73-8
Boc-Dab(Alloc)-OH

Guidance literature:: Multi-step reaction with 2 steps

1: [bis(acetoxy)iodo]benzene / water; acetonitrile; ethyl acetate / Heating

2: potassium carbonate / water; diethyl ether / 20 °C

With [bis(acetoxy)iodo]benzene; potassium carbonate; In diethyl ether; water; ethyl acetate; acetonitrile;
DOI:10.1055/s-0036-1588393