(R)-Ν-(1-phenylethyl)methanesulfonamide

Base Information

Chemical Name:(R)-Ν-(1-phenylethyl)methanesulfonamide
CAS No.:316363-65-2
Molecular Formula:C₉H₁₃NO₂S
Molecular Weight:199.274
Hs Code.:

Synonyms:(R)-Ν-(1-phenylethyl)methanesulfonamide

Suppliers and Price of (R)-Ν-(1-phenylethyl)methanesulfonamide

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

TRC
N-[(R)-1-Phenylethyl]-methanesulfonamide
1g
$ 1260.00

TRC
N-[(R)-1-Phenylethyl]-methanesulfonamide
100mg
$ 160.00

Total 7 raw suppliers

Chemical Property of (R)-Ν-(1-phenylethyl)methanesulfonamide

Chemical Property:

Purity/Quality:

>95% ^*data from raw suppliers

N-[(R)-1-Phenylethyl]-methanesulfonamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses N-[(R)-1-Phenylethyl]-methanesulfonamide is a reactant used in the extremely efficient synthesis of N-acyl sulfunamides.

Technology Process of (R)-Ν-(1-phenylethyl)methanesulfonamide

There total 5 articles about (R)-Ν-(1-phenylethyl)methanesulfonamide 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: 99.0%

: 3886-69-9
(R)-1-phenyl-ethyl-amine

: 124-63-0
methanesulfonyl chloride

: 316363-65-2
(R)-Ν-(1-phenylethyl)methanesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1002/adsc.201500905

Reference yield: 82.0%

: 69380-83-2
N-(1-phenylethylidene)methanesulfonamide

: 316363-65-2
(R)-Ν-(1-phenylethyl)methanesulfonamide

Guidance literature:: With hydrogen; silver trifluoromethanesulfonate; palladium diacetate; (R)-(6,6′-dimethoxy-[1,1′-biphenyl]-2,2′-diyl)bis(diphenylphosphine); In 1,2-dichloro-ethane; at 70 ℃; for 66h; under 760.051 Torr; enantioselective reaction; Schlenk technique;
DOI:10.1002/ejoc.201801123

Reference yield:

: 544-97-8
dimethyl zinc(II)

: 73845-05-3
(E)-N-benzylidenemethanesulfonamide

: 193482-26-7
(S)-N-(1-phenylethyl) methanesulfonamide

: 316363-65-2
(R)-Ν-(1-phenylethyl)methanesulfonamide

Guidance literature:: With copper(II) bis(trifluoromethanesulfonate); (S)-1-[2-diphenylphosphinomethyl-4,4-bis(2,4,6-triisopropylphenylmethyl)pyrrolidin-1-yl]-2,2-dimethylpropan-1-one; In toluene; at 20 ℃; for 20h; Title compound not separated from byproducts;
DOI:10.1021/jo035234q