2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid

Base Information

Chemical Name:2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid
CAS No.:119479-32-2
Molecular Formula:C10H17NO4
Molecular Weight:215.249
Hs Code.:2924199090
European Community (EC) Number:845-933-1
DSSTox Substance ID:DTXSID10409080
Nikkaji Number:J686.564J
Mol file:119479-32-2.mol

Synonyms:119479-32-2;2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid;2-(TERT-BUTOXYCARBONYLAMINO)PENT-4-ENOIC ACID;2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-enoic Acid;4-Pentenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-;2-{[(tert-butoxy)carbonyl]amino}pent-4-enoic acid;2-(Boc-amino)-4-pentenoic acid;2-((tert-Butoxycarbonyl)amino)pent-4-enoicacid;2-(BOC-AMINO)PENT-4-ENOIC ACID;2-[(tert-butoxycarbonyl)amino]pent-4-enoic acid;MFCD01320851;N-Boc-2-allyl-L-glycine;SCHEMBL212773;DTXSID10409080;BUPDPLXLAKNJMI-UHFFFAOYSA-N;AR3176;MFCD02682445;N-tert-Butoxycarbonyl-dl-allylglycine;AKOS013465630;SS-4916;AM803025;PD197008;SY035326;2-tert-butoxycarbonylamino-pent-4-enoic acid;CS-0170866;FT-0649586;FT-0658051;EN300-118378;2-[(tert-butoxycarbonyl)amino]-4-pentenoic acid;A857824;F2147-6511;Z1201004872;2-(tert-butoxycarbonyl)pent-4-enoic acid

Suppliers and Price of 2-((tert-Butoxycarbonyl)amino)pent-4-enoic 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
2-(tert-Butoxycarbonylamino)pent-4-enoicAcid
100mg
$ 220.00

SynQuest Laboratories
2-{[(tert-Butoxy)carbonyl]amino}pent-4-enoic acid
500 mg
$ 352.00

Matrix Scientific
2-{[(tert-Butoxy)carbonyl]amino}pent-4-enoicacid >95%
1g
$ 532.00

Matrix Scientific
2-{[(tert-Butoxy)carbonyl]amino}pent-4-enoicacid >95%
500mg
$ 393.00

Crysdot
2-((tert-Butoxycarbonyl)amino)pent-4-enoicacid 95+%
5g
$ 715.00

Chemenu
2-{[(tert-Butoxy)carbonyl]amino}pent-4-enoicacid 95%
5g
$ 669.00

Biosynth Carbosynth
2-(Tert-Butoxycarbonylamino)Pent-4-Enoic Acid
1 g
$ 416.00

Biosynth Carbosynth
2-(Tert-Butoxycarbonylamino)Pent-4-Enoic Acid
2 g
$ 665.60

Biosynth Carbosynth
2-(Tert-Butoxycarbonylamino)Pent-4-Enoic Acid
250 mg
$ 115.00

Biosynth Carbosynth
2-(Tert-Butoxycarbonylamino)Pent-4-Enoic Acid
100 mg
$ 93.00

Total 17 raw suppliers

Chemical Property of 2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid

Chemical Property:

Melting Point:109 °C(Solv: dichloromethane (75-09-2); pentane (109-66-0))
Boiling Point:352.0±35.0 °C(Predicted)
PKA:3.83±0.10(Predicted)
PSA：79.12000
Density:1.097±0.06 g/cm3(Predicted)
LogP:1.74480
Storage Temp.:2-8°C(protect from light)
XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:215.11575802
Heavy Atom Count:15
Complexity:255

Purity/Quality:

97% ^*data from raw suppliers

2-(tert-Butoxycarbonylamino)pent-4-enoicAcid ^*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(CC=C)C(=O)O

Technology Process of 2-((tert-Butoxycarbonyl)amino)pent-4-enoic acid

There total 15 articles about 2-((tert-Butoxycarbonyl)amino)pent-4-enoic 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: 100.0%

: 124373-83-7
allyl 2-(tert-butoxycarbonylamino)acetate

: 119479-32-2
2-((tert-butyloxycarbonyl)amino)-4-pentenoic acid

Guidance literature:: allyl 2-(tert-butoxycarbonylamino)acetate; With aluminum isopropoxide; quinidine; In tetrahydrofuran; at -78 ℃; Inert atmosphere;

With n-butyllithium; 1,1,1,3,3,3-hexamethyl-disilazane; In tetrahydrofuran; hexane; at 20 ℃; for 12.3333h; Inert atmosphere;
DOI:10.1039/c3ob41215f