(R)-tert-butyl (1-oxopentan-3-yl)carbamate

Base Information

Chemical Name:(R)-tert-butyl (1-oxopentan-3-yl)carbamate
CAS No.:198493-29-7
Molecular Formula:C₁₀H₁₉NO₃
Molecular Weight:201.266
Hs Code.:
DSSTox Substance ID:DTXSID601207259
Nikkaji Number:J897.783F
Mol file:198493-29-7.mol

Synonyms:198493-29-7;Tert-butyl N-[(3R)-1-oxopentan-3-yl]carbamate;Carbamic acid, [(1R)-1-ethyl-3-oxopropyl]-, 1,1-dimethylethyl ester (9CI);(R)-tert-butyl (1-oxopentan-3-yl)carbamate;SCHEMBL1722623;VEVHRUHHMAZBRX-MRVPVSSYSA-N;DTXSID601207259;(3R)-3-[(tert-Butyloxycarbonyl)amino]pentanal;EN300-6262601;((R)-1-ethyl-3-oxo-propyl)carbamic acid tert-butyl ester;1,1-Dimethylethyl N-[(1R)-1-ethyl-3-oxopropyl]carbamate

Suppliers and Price of (R)-tert-butyl (1-oxopentan-3-yl)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
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price

Total 1 raw suppliers

Chemical Property of (R)-tert-butyl (1-oxopentan-3-yl)carbamate

Chemical Property:

PSA：55.40000
LogP:2.26960
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:201.13649347
Heavy Atom Count:14
Complexity:196

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(CC=O)NC(=O)OC(C)(C)C
Isomeric SMILES:CC[C@H](CC=O)NC(=O)OC(C)(C)C

Technology Process of (R)-tert-butyl (1-oxopentan-3-yl)carbamate

There total 4 articles about (R)-tert-butyl (1-oxopentan-3-yl)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: 68.0%

: 198493-28-6
(R)-N-tert-butyloxycarbonyl-3-aminopentanenitrile

: 198493-29-7
((R)-1-ethyl-3-oxo-propyl)-carbamic acid tert-butyl ester

Guidance literature:: With diisobutylaluminium hydride; In diethyl ether; toluene; at -60 ℃; for 7.5h;

Reference yield:

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

: 198493-29-7
((R)-1-ethyl-3-oxo-propyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / Ambient temperature

2: TEA / CH₂Cl₂ / Ambient temperature

3: dimethylsulfoxide / 45 °C

4: 68 percent / DIBAL-H / toluene; diethyl ether / 7.5 h / -60 °C

With TEA; diisobutylaluminium hydride; In tetrahydrofuran; diethyl ether; dichloromethane; dimethyl sulfoxide; toluene;

Reference yield:

: 150736-71-3
tert-butyl (R)-(1-hydroxybutan-2-yl)carbamate

: 198493-29-7
((R)-1-ethyl-3-oxo-propyl)-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: TEA / CH₂Cl₂ / Ambient temperature

2: dimethylsulfoxide / 45 °C

3: 68 percent / DIBAL-H / toluene; diethyl ether / 7.5 h / -60 °C

With TEA; diisobutylaluminium hydride; In diethyl ether; dichloromethane; dimethyl sulfoxide; toluene;