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tert-Butyl azetidin-3-ylcarbamate

Base Information Edit
  • Chemical Name:tert-Butyl azetidin-3-ylcarbamate
  • CAS No.:91188-13-5
  • Molecular Formula:C8H16N2O2
  • Molecular Weight:172.227
  • Hs Code.:2933990090
  • European Community (EC) Number:676-108-2
  • DSSTox Substance ID:DTXSID50364023
  • Nikkaji Number:J3.174.967K
  • Wikidata:Q72447817
  • Mol file:91188-13-5.mol
tert-Butyl azetidin-3-ylcarbamate

Synonyms:91188-13-5;tert-Butyl azetidin-3-ylcarbamate;3-N-Boc-amino-azetidine;3-Boc-aminoazetidine;3-(boc-amino)azetidine;3-N-Boc-aminoazetidine;Tert-butyl N-(azetidin-3-yl)carbamate;3-(n-boc-amino)azetidine;Azetidin-3-yl-carbamic acid tert-butyl ester;tert-butyl N-azetidin-3-ylcarbamate;MFCD01861759;Carbamic acid, 3-azetidinyl-, 1,1-dimethylethyl ester;3-(BOC-AMINO)-AZETIDINE;3-(tert-butoxycarbonylamino)azetidine;3-[(tert-Butoxycarbonyl)amino]azetidine;SCHEMBL114920;t-butyl azetidin-3-ylcarbamate;tert-Butyl 3-azetidinylcarbamate;tert-Butylazetidin-3-ylcarbamate;DTXSID50364023;3-tert-butoxycarbonylaminoazetidine;tert.-butyl-azetidin-3-ylcarbamate;BCP05247;3-N-Boc-amino-azetidine, AldrichCPR;AKOS005146174;CS-W008685;PS-5674;1,1-dimethylethyl 3-azetidinylcarbamate;1,1-dimethylethyl azetidin-3-ylcarbamate;SY017239;azetidin-3-ylcarbamic acid tert-butyl ester;azetidin-3-yl-carbamic acid tert butyl ester;azetidine-3-ylcarbamic acid tert-butyl ester;FT-0648214;EN300-80654;N-(3-Azetidinyl)carbamic acid tert-butyl ester;3-azetidinyl-carbamic acid, 1,1-dimethylethyl ester;Q-103146

Suppliers and Price of tert-Butyl azetidin-3-ylcarbamate
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
  • tert-ButylN-Azetidin-3-ylcarbamate
  • 50mg
  • $ 85.00
  • Synthonix
  • 3-(Boc-amino)azetidine 95+%
  • 250mg
  • $ 15.00
  • Synthonix
  • 3-(Boc-amino)azetidine 95+%
  • 1g
  • $ 30.00
  • Synthonix
  • 3-(Boc-amino)azetidine 95+%
  • 5g
  • $ 100.00
  • Synthonix
  • 3-(Boc-amino)azetidine 95+%
  • 10g
  • $ 200.00
  • SynChem
  • 3-N-BOC-AMINO-AZETIDINE 95%
  • 1 g
  • $ 150.00
  • Sigma-Aldrich
  • 3-(Boc-amino)azetidine
  • 500mg
  • $ 94.90
  • Matrix Scientific
  • 3-N-Boc-Aminoazetidine 98%
  • 25g
  • $ 860.00
  • Matrix Scientific
  • 3-N-Boc-Aminoazetidine 98%
  • 5g
  • $ 259.00
  • Chemcia Scientific
  • 3-N-Boc-AminoazetidineAcetate 95%
  • 2 G
  • $ 185.00
Total 91 raw suppliers
Chemical Property of tert-Butyl azetidin-3-ylcarbamate Edit
Chemical Property:
  • Appearance/Colour:white powder 
  • Melting Point:63-72°C 
  • Refractive Index:1.49 
  • Boiling Point:267.5 °C at 760 mmHg 
  • PKA:12.26±0.40(Predicted) 
  • Flash Point:115.6 °C 
  • PSA:50.36000 
  • Density:1.06 g/cm3 
  • LogP:1.20260 
  • Storage Temp.:Keep in dark place,Sealed in dry,Room Temperature 
  • Water Solubility.:Soluble in water. (5g/100ml) 
  • XLogP3:0.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:172.121177757
  • Heavy Atom Count:12
  • Complexity:170
Purity/Quality:

99% *data from raw suppliers

tert-ButylN-Azetidin-3-ylcarbamate *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38-52 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NC1CNC1
  • Uses tert-Butyl N-Azetidin-3-ylcarbamate is a versatile reactant used in the preparation of substituted benzothiazoles via copper-catalyzed three-component domino condensation/S-arylation/heterocyclization reactions. Also used in the synthesis and pharmacokinetic evaluation of Et aminonicotinate sulfonylureas as antagonists of P2Y12 receptor.
Technology Process of tert-Butyl azetidin-3-ylcarbamate

There total 2 articles about tert-Butyl azetidin-3-ylcarbamate 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 hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; for 2h;
Guidance literature:
Refernces Edit
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