4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide

Base Information

Chemical Name:4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide
CAS No.:122012-96-8
Molecular Formula:C₁₃H₁₇NO₂S
Molecular Weight:251.349
Hs Code.:
DSSTox Substance ID:DTXSID20579829
Wikidata:Q82470461
Mol file:122012-96-8.mol

Synonyms:122012-96-8;4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide;DTXSID20579829

Suppliers and Price of 4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:251.09799996
Heavy Atom Count:17
Complexity:260

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C(=O)CC(=O)CSCC1=CC=CC=C1

Technology Process of 4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide

There total 1 articles about 4-(Benzylsulfanyl)-N,N-dimethyl-3-oxobutanamide 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: 80.0%

: 3492-64-6
sodium benzylmercaptide

: 122013-04-1
γ-bromo-N,N-dimethylacetoacetamide

: 122012-96-8
4-benzylthio-N,N-dimethylacetoacetamide

Guidance literature:: In isopropyl alcohol; for 1h; Ambient temperature;

Reference yield: 51.0%

: 14204-23-0
N-(benzylthio)succinimide

: 122012-96-8
4-benzylthio-N,N-dimethylacetoacetamide

: 122012-95-7
2,4-bis(benzylthio)-N,N-dimethylacetoacetamide

Guidance literature:: With triethylamine; In dichloromethane; for 24h; Ambient temperature;

Reference yield:

: 122012-96-8
4-benzylthio-N,N-dimethylacetoacetamide

: 122012-97-9,122012-98-0
anti-2,4-bis(benzylthio)-3-hydroxy-N,N-dimethylbutyramide

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / Et₃N / CH₂Cl₂ / 24 h / Ambient temperature

2: 40.9 percent / NaBH₄ / ethanol / 0.33 h / Ambient temperature

With sodium tetrahydroborate; triethylamine; In ethanol; dichloromethane;