Decanoic acid, 2-amino-8-oxo-, (2S)-

Base Information

Chemical Name:Decanoic acid, 2-amino-8-oxo-, (2S)-
CAS No.:375858-14-3
Molecular Formula:C10H19NO3
Molecular Weight:201.266
Hs Code.:
DSSTox Substance ID:DTXSID00470941
Nikkaji Number:J1.960.785B
Mol file:375858-14-3.mol

Synonyms:L-2-amino-8-oxodecanoic acid;Decanoic acid, 2-amino-8-oxo-, (2S)-;375858-14-3;(s)-2-amino-8-oxodecanoic acid;SCHEMBL7791775;DTXSID00470941

Suppliers and Price of Decanoic acid, 2-amino-8-oxo-, (2S)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Decanoic acid, 2-amino-8-oxo-, (2S)-

Chemical Property:

XLogP3:-1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:201.13649347
Heavy Atom Count:14
Complexity:192

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(=O)CCCCCC(C(=O)O)N
Isomeric SMILES:CCC(=O)CCCCC[C@@H](C(=O)O)N

Technology Process of Decanoic acid, 2-amino-8-oxo-, (2S)-

There total 1 articles about Decanoic acid, 2-amino-8-oxo-, (2S)- 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:

: 183506-66-3
apicidin

: 375858-14-3
(2S)-2-amino-8-oxodecanoic acid

: 73-32-5,959215-79-3,18875-42-8
L-isoleucine

: 1723-00-8,83680-83-5
(R)-(+)-pipecolic acid

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

Guidance literature:: With hydrogenchloride; water; mercaptoacetic acid; at 110 ℃; for 8h; Inert atmosphere; Sealed tube;
DOI:10.1021/np4006053