tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate

Base Information

Chemical Name:tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate
CAS No.:149876-86-8
Molecular Formula:C₁₃H₂₇N₃O₄
Molecular Weight:289.375
Hs Code.:
European Community (EC) Number:849-806-1
Nikkaji Number:J1.368.408A

Synonyms:149876-86-8;tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate;Di-tert-butyl (2-aminopropane-1,3-diyl)dicarbamate;tert-butyl N-[2-amino-3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]carbamate;1,3-Di-(N-Boc-amino)-2-aminopropane;SCHEMBL2748354;QYVFEFFJTQKDTK-UHFFFAOYSA-N;MFCD24465597;AKOS033771891;Tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl) Carbamate;BS-45798;CS-0139144;C77442;EN300-216352;Di-t-butyl (2-aminopropane-1,3-diyl)dicarbamate;Di-tert-butyl(2-aminopropane-1,3-diyl)dicarbamate;di-tert-butyl(2-aminopropane-1,3-diyl)biscarbamate;di-tert-butyl (2-amino-1,3-propanediyl)biscarbamate;Di-tert-butyl (2-aminopropane-1,3-diyl)biscarbamate;Z1508686114

Suppliers and Price of tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate

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
tert-butylN-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate
50mg
$ 240.00

AK Scientific
Tert-butylN-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate
10g
$ 4492.00

Acrotein
1,3-Di-(N-Boc-amino)-2-aminopropane 97%
1g
$ 330.00

Acrotein
1,3-Di-(N-Boc-amino)-2-aminopropane 97%
0.5g
$ 220.00

Total 3 raw suppliers

Chemical Property of tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:289.20015635
Heavy Atom Count:20
Complexity:300

Purity/Quality:

99% ^*data from raw suppliers

tert-butylN-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NCC(CNC(=O)OC(C)(C)C)N
Uses tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate is a reactant or reagent in synthesis, and biological evaluation of glycodendrimer-?cyclodextrin conjugates.

Technology Process of tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate

There total 6 articles about tert-butyl N-(2-amino-3-{[(tert-butoxy)carbonyl]amino}propyl)carbamate 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: 90.0%

: 149876-85-7
di-tert-butyl (2-azidopropane-1,3-diyl)dicarbamate

: 149876-86-8
di-tert-butyl (2-aminopropane-1,3-diyl)dicarbamate

Guidance literature:: With tin(ll) chloride; In methanol; for 1h; Ambient temperature;
DOI:10.1055/s-1998-2128

Reference yield:

: 848770-45-6
di-tert-butyl [2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1,3-propanediyl]biscarbamate

: 149876-86-8
di-tert-butyl (2-aminopropane-1,3-diyl)dicarbamate

Guidance literature:: With hydrazine; In ethanol; at 0 ℃; for 5h; Heating / reflux;

Reference yield:

: 98642-15-0
(3-tert-butoxycarbonylamino-2-hydroxy-propyl)-carbamic acid tert-butyl ester

: 149876-86-8
di-tert-butyl (2-aminopropane-1,3-diyl)dicarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / Et₃N / CH₂Cl₂ / 1 h / 20 °C

2: 94 percent / NaN₃ / dimethylformamide / 18 h / 100 °C

3: 82 percent / H₂ / Pd/C / methanol / 18 h / 2327.17 Torr

With sodium azide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm040208l