(2S)-N-benzyl-2-hydroxy-3-methylbutanamide

Base Information

Chemical Name:(2S)-N-benzyl-2-hydroxy-3-methylbutanamide
CAS No.:179923-30-9
Molecular Formula:C12H17NO2
Molecular Weight:207.272
Hs Code.:
DSSTox Substance ID:DTXSID70443400
Nikkaji Number:J51.983I
Wikidata:Q82261184
Mol file:179923-30-9.mol

Synonyms:CTK0A6674;179923-30-9;DTXSID70443400;[S,(?)]-N-Benzyl-2-hydroxy-3-methylbutyramide

Suppliers and Price of (2S)-N-benzyl-2-hydroxy-3-methylbutanamide

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

Total 1 raw suppliers

Chemical Property of (2S)-N-benzyl-2-hydroxy-3-methylbutanamide

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:207.125928785
Heavy Atom Count:15
Complexity:198

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(=O)NCC1=CC=CC=C1)O
Isomeric SMILES:CC(C)[C@@H](C(=O)NCC1=CC=CC=C1)O

Technology Process of (2S)-N-benzyl-2-hydroxy-3-methylbutanamide

There total 8 articles about (2S)-N-benzyl-2-hydroxy-3-methylbutanamide 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: 83.0%

: 17407-55-5
(S)-2-Hydroxy-3-methylbutanoic acid

: 100-46-9
benzylamine

: 179923-30-9
(S)-N-benzyl-2-hydroxy-3-methylbutanamide

Guidance literature:: With 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 0 - 20 ℃; for 20.25h;
DOI:10.1002/anie.201712829

Reference yield: 58.0%

: N-benzyl-2-hydroxy-3-methylbutyramide

: 262369-97-1
N-benzyl-3-methyl-2-oxobutanamide

: (R)-N-benzyl-2-hydroxy-3-methylbutyramide

: 179923-30-9
(S)-N-benzyl-2-hydroxy-3-methylbutanamide

Guidance literature:: With oxygen; In chloroform; at 40 ℃; for 95h; enantioselective reaction; Resolution of racemate;
DOI:10.1002/adsc.201100062