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(S)-N-Boc-2,3-epoxypropylamine

Base Information Edit
  • Chemical Name:(S)-N-Boc-2,3-epoxypropylamine
  • CAS No.:161513-47-9
  • Molecular Formula:C8H15NO3
  • Molecular Weight:173.212
  • Hs Code.:2924199090
  • European Community (EC) Number:605-257-8
  • DSSTox Substance ID:DTXSID701218168
  • Wikidata:Q76415072
  • Mol file:161513-47-9.mol
(S)-N-Boc-2,3-epoxypropylamine

Synonyms:161513-47-9;(S)-N-Boc-2,3-epoxypropylamine;(s)-1-(tert-butoxycarbonyl)-2,3-oxiranylmethylamine;tert-butyl N-[[(2S)-oxiran-2-yl]methyl]carbamate;tert-butyl N-{[(2S)-oxiran-2-yl]methyl}carbamate;(s)-tert-butyl oxiran-2-ylmethylcarbamate;Carbamic acid, [(2S)-oxiranylmethyl]-, 1,1-dimethylethyl ester;Carbamic acid, N-[(2S)-2-oxiranylmethyl]-, 1,1-dimethylethyl ester;starbld0018309;SCHEMBL2750096;ZBBGKXNNTNBRBH-LURJTMIESA-N;DTXSID701218168;AKOS028109283;tert-butyl (2S)oxiranylmethylcarbamate;(S)-N-Boc-2,3-epoxypropylamine, 97%;AS-72044;tert-butyl (2S)-oxiran-2-ylmethylcarbamate;CS-0132706;tert-Butyl (S)-(oxiran-2-ylmethyl)carbamate;D85839;EN300-1879354;(S)-1-(t-Butoxycarbonyl)-2,3-oxiranylmethylamine;(S)-oxiranylmethyl-carbamic acid tert-butyl ester;J-200125;1,1-Dimethylethyl N-[(2S)-2-oxiranylmethyl]carbamate

Suppliers and Price of (S)-N-Boc-2,3-epoxypropylamine
Supply Marketing:Edit
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
  • (S)-N-Boc-2,3-epoxypropylamine
  • 500mg
  • $ 330.00
  • TRC
  • (S)-N-Boc-2,3-epoxypropylamine
  • 100mg
  • $ 85.00
  • Sigma-Aldrich
  • (S)-N-Boc-2,3-epoxypropylamine 97%
  • 250mg
  • $ 79.70
  • Sigma-Aldrich
  • (S)-N-Boc-2,3-epoxypropylamine 97%
  • 1g
  • $ 352.00
  • American Custom Chemicals Corporation
  • (S)-1-(TERT-BUTOXYCARBONYL)-2,3-OXIRANYLMETHYLAMINE 95.00%
  • 1G
  • $ 878.03
  • American Custom Chemicals Corporation
  • (S)-1-(TERT-BUTOXYCARBONYL)-2,3-OXIRANYLMETHYLAMINE 95.00%
  • 250MG
  • $ 629.42
  • ACHEMBLOCK
  • (S)-1-(tert-Butoxycarbonyl)-2,3-oxiranylamine 95%
  • 5G
  • $ 1050.00
  • ACHEMBLOCK
  • (S)-1-(tert-Butoxycarbonyl)-2,3-oxiranylamine 95%
  • 1G
  • $ 350.00
Total 23 raw suppliers
Chemical Property of (S)-N-Boc-2,3-epoxypropylamine Edit
Chemical Property:
  • Vapor Pressure:0.011mmHg at 25°C 
  • Melting Point:48-50 °C 
  • Refractive Index:1.462 
  • Boiling Point:262.908 °C at 760 mmHg 
  • PKA:12.45±0.46(Predicted) 
  • Flash Point:112.803 °C 
  • PSA:50.86000 
  • Density:1.081 g/cm3 
  • LogP:1.30080 
  • XLogP3:0.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:173.10519334
  • Heavy Atom Count:12
  • Complexity:174
Purity/Quality:

90.0%Min *data from raw suppliers

(S)-N-Boc-2,3-epoxypropylamine *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NCC1CO1
  • Isomeric SMILES:CC(C)(C)OC(=O)NC[C@H]1CO1
  • Uses (S)-N-Boc-2,3-epoxypropylamine can be used:To functionalize detonation nanodiamonds with NH2 functional group to enhance their optical properties.In the synthesis of poly(ethylene glycol) (PEG) based block copolymers, which are further used in the preparation of micelles loaded with mRNA for intracellular mRNA delivery.
Technology Process of (S)-N-Boc-2,3-epoxypropylamine

There total 11 articles about (S)-N-Boc-2,3-epoxypropylamine 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:
Guidance literature:
With lithium tert-butoxide; In methanol;
DOI:10.1021/op034028h
Guidance literature:
With potassium carbonate; In methanol; at 20 ℃; for 3h;
Guidance literature:
With sodium methylate; In methanol; for 3h; Ambient temperature;
DOI:10.1021/jm00048a007
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