tert-Butyl (3-oxocyclopentyl)carbamate

Base Information

Chemical Name:tert-Butyl (3-oxocyclopentyl)carbamate
CAS No.:847416-99-3
Molecular Formula:C10H17NO3
Molecular Weight:199.25
Hs Code.:2924299090
European Community (EC) Number:845-028-1
DSSTox Substance ID:DTXSID90699482
Mol file:847416-99-3.mol

Synonyms:847416-99-3;tert-Butyl (3-oxocyclopentyl)carbamate;tert-butyl 3-oxocyclopentylcarbamate;3-(BOC-AMINO)CYCLOPENTANONE;TERT-BUTYL N-(3-OXOCYCLOPENTYL)CARBAMATE;(3-OXO-CYCLOPENTYL)-CARBAMIC ACID TERT-BUTYL ESTER;MFCD09751875;tert-butyl(3-oxocyclopentyl)carbamate;Carbamic acid, (3-oxocyclopentyl)-, 1,1-dimethylethyl ester;1-(BOC-AMINO)-3-OXOCYCLOPENTANE;MFCD18089809;(S)-3-(BOC-AMINO)CYCLOPENTANONE;3-Methylphenylaceticacid;SCHEMBL720530;3-(Boc-amino)cyclopentan-1-one;DTXSID90699482;CLOXAWYNXXEWBT-UHFFFAOYSA-N;3-N-BOC-AMINOCYCLOPENTANONE;AMY35565;BCP22363;AKOS006326261;CS-W004951;PB18261;PB22919;PB31383;DS-16811;SY017241;SY111850;FT-0660817;EN300-98970;A854002;(3-Oxo-cyclopentyl)-carbamic acid tert-butyl ester, AldrichCPR

Suppliers and Price of tert-Butyl (3-oxocyclopentyl)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

Usbiological
ML 213
10mg
$ 423.00

TRC
3-(Boc-amino)cyclopentanone
500mg
$ 155.00

Tocris
ML213 ≥99%(HPLC)
50
$ 785.00

Tocris
ML213 ≥99%(HPLC)
10
$ 184.00

SynQuest Laboratories
tert-Butyl N-(3-oxocyclopentyl)carbamate 97.0%
25 g
$ 1790.00

SynQuest Laboratories
tert-Butyl N-(3-oxocyclopentyl)carbamate 97.0%
5 g
$ 1090.00

SynQuest Laboratories
tert-Butyl N-(3-oxocyclopentyl)carbamate 97.0%
250 mg
$ 125.00

SynQuest Laboratories
tert-Butyl N-(3-oxocyclopentyl)carbamate 97.0%
1 g
$ 365.00

Sigma-Aldrich
ML213 ≥98% (HPLC)
25 mg
$ 311.00

Sigma-Aldrich
ML213 ≥98% (HPLC)
5 mg
$ 80.50

Total 35 raw suppliers

Chemical Property of tert-Butyl (3-oxocyclopentyl)carbamate

Chemical Property:

Boiling Point:319.2±31.0 °C(Predicted)
PKA:11.89±0.20(Predicted)
PSA：58.89000
Density:1.07±0.1 g/cm3(Predicted)
LogP:1.83710
Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C
XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:199.12084340
Heavy Atom Count:14
Complexity:242

Purity/Quality:

97% ^*data from raw suppliers

ML 213 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC1CCC(=O)C1

Technology Process of tert-Butyl (3-oxocyclopentyl)carbamate

There total 8 articles about tert-Butyl (3-oxocyclopentyl)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: 99.0%

: 1154870-59-3,207729-04-2
trans-(+/-)-(3-hydroxycyclopentyl)-carbamic acid,1,1-dimethylethyl ester

: 847416-99-3
tert-butyl N-(3-oxocyclopentyl)carbamate

Guidance literature:: With Dess-Martin periodane; In dichloromethane; at 0 - 20 ℃; for 19h;

Reference yield: 69.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 3-azido-cyclopentan-1-one

: 847416-99-3
tert-butyl N-(3-oxocyclopentyl)carbamate

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethyl acetate; for 18h;

Reference yield: 60.0%

: 855863-93-3
3-tert-butoxycarbonylaminocyclopentanecarboxylic acid

: 847416-99-3
tert-butyl N-(3-oxocyclopentyl)carbamate

Guidance literature:: With (2,2'-dipyridyl)bis(5-methyl-2-(4-fluoro)phenylpyridine-N,C)iridium(III) hexafluorophosphate; oxygen; sodium carbonate; 1,1'-diethyl-4,4'-bipyridinium diperchlorate; In dimethyl sulfoxide; at 20 ℃; for 16h; under 760.051 Torr; Irradiation;
DOI:10.1002/ijch.201900130