(S)-3-Aminovaleric acid ethyl ester

Base Information

Chemical Name:(S)-3-Aminovaleric acid ethyl ester
CAS No.:470707-09-6
Molecular Formula:C7H15NO2
Molecular Weight:145.202
Hs Code.:
DSSTox Substance ID:DTXSID40460780
Nikkaji Number:J1.625.035J
Wikidata:Q82284928
Mol file:470707-09-6.mol

Synonyms:ETHYL (3S)-3-AMINOPENTANOATE;(S)-3-AMINOVALERIC ACID ETHYL ESTER;DTXSID40460780;EN300-4296269

Suppliers and Price of (S)-3-Aminovaleric acid ethyl ester

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

American Custom Chemicals Corporation
(S)-3-AMINOVALERIC ACIDETHYL ESTER 95.00%
5MG
$ 495.31

Total 0 raw suppliers

Chemical Property of (S)-3-Aminovaleric acid ethyl ester

Chemical Property:

PSA：52.32000
LogP:1.37720
XLogP3:0.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:145.110278721
Heavy Atom Count:10
Complexity:104

Purity/Quality:: (S)-3-AMINOVALERIC ACIDETHYL ESTER 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(CC(=O)OCC)N
Isomeric SMILES:CC[C@@H](CC(=O)OCC)N

Technology Process of (S)-3-Aminovaleric acid ethyl ester

There total 5 articles about (S)-3-Aminovaleric acid ethyl ester 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: 9.0%

: 75-31-0
isopropylamine

: 4949-44-4
ethyl propanoylacetate

: 470707-09-6
(S)-3-Amino-pentanoic acid ethyl ester

: 98-86-2
acetophenone

Guidance literature:: With pyridoxal 5'-phosphate; recombinant ω-transaminase from Burkholderia vietnamiensis G4; In aq. phosphate buffer; at 37 ℃; for 12h; pH=7.4; Time; enantioselective reaction; Enzymatic reaction;
DOI:10.1016/j.molcatb.2013.11.013

Reference yield:

: 2627-86-3
(S)-1-phenyl-ethylamine

: 4949-44-4
ethyl propanoylacetate

: 470707-09-6
(S)-3-Amino-pentanoic acid ethyl ester

: 98-86-2
acetophenone

Guidance literature:: With pyridoxal 5'-phosphate; recombinant ω-transaminase from Burkholderia vietnamiensis G4; In aq. phosphate buffer; at 37 ℃; for 12h; pH=7.4; Time; enantioselective reaction; Enzymatic reaction;
DOI:10.1016/j.molcatb.2013.11.013

Reference yield:

: 142342-62-9,142342-70-9
3-[Benzyl-((R)-2-hydroxy-1-phenyl-ethyl)-amino]-pentanoic acid ethyl ester

: 142342-74-3
(R)-3-amino-valeric acid ethyl ester

: 470707-09-6
(S)-3-Amino-pentanoic acid ethyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; under 6750.5 Torr; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
DOI:10.1016/S0040-4039(00)78889-7