Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)-

Base Information

Chemical Name:Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)-
CAS No.:56762-94-8
Molecular Formula:C₁₃H₁₇NO₅S
Molecular Weight:299.348
Hs Code.:
DSSTox Substance ID:DTXSID101151895

Synonyms:DTXSID101151895;Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)-;56762-94-8

Suppliers and Price of Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)-

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 Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)-

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:7
Exact Mass:299.08274382
Heavy Atom Count:20
Complexity:434

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C(CCS(=O)(=O)C)NC(=O)C1=CC=CC=C1
Isomeric SMILES:COC(=O)[C@H](CCS(=O)(=O)C)NC(=O)C1=CC=CC=C1

Technology Process of Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)-

There total 3 articles about Butanoic acid, 2-(benzoylamino)-4-(methylsulfonyl)-, methyl ester, (S)- 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: 48.0%

: 50732-06-4
methyl benzoyl-L-methioninate

: 82933-21-9
N-benzoyl-L-aspartic acid α-methyl ester

: 115527-63-4,1163291-88-0
Bz-Met(sulfone)-OH

: 56762-94-8
Bz-Met(sulfone)-OMe

Guidance literature:: With 4-^tButyl iodoxybenzene; In chlorobenzene; for 3h; Heating;
DOI:10.1016/S0040-4020(01)87715-2

Reference yield: 29.0%

: 50732-06-4
methyl benzoyl-L-methioninate

: 3054-52-2,39608-56-5,39608-57-6,115589-95-2
N-benzoyl L-methionine sulphoxide

: 56782-76-4
Bz-Met(sulfoxide)-OMe

: 115527-64-5
BzNHCH(CH₂CH₂SO₂H)COOMe

: 56762-94-8
Bz-Met(sulfone)-OMe

Guidance literature:: With 4-^tButyl iodoxybenzene; In chlorobenzene; for 3h; Further byproducts given; Heating;
DOI:10.1016/S0040-4020(01)87715-2

Reference yield:

: 2491-18-1
(S)-methyl 2-amino-4-(methylthio)butanoate hydrochloride

: 56762-94-8
Bz-Met(sulfone)-OMe

Guidance literature:: Multi-step reaction with 2 steps

1: aq. bicarbonate / benzoylation

2: 29 percent / 4-t-butyl iodoxybenzene / chlorobenzene / 3 h / Heating

With bicarbonate; 4-^tButyl iodoxybenzene; In chlorobenzene;
DOI:10.1016/S0040-4020(01)87715-2