(R)-(+)-tert-Butylsulfinamide CAS 196929-78-9 Puritas ≥99.0% ee≥99.0% Manufacturer Alta Puritas
Manufacturer Supple cum High puritate et stabulo Quality
(R)-(+)-tert-Butylsulfinamide CAS 196929-78-9
(S)-(-)-tert-Butylsulfinamide CAS 343338-28-3
Chiral Compounds, High Quality, Commercial Production
Nomen chemicum | (R)-(+)-tert-Butylsulfinamide |
Synonyma | (R)-(+)-2-Methyl-2-Propanesulfinamide;R-BSN |
CAS Number | 196929-78-9 |
CATTUS Number | RF-CC218 |
Stock Status | In Stock, Productio Ascendite ad Tons |
Formulae hypotheticae | C4H11NOS |
M. Pondus | 121.2 |
Liquescens punctum | 103.0~ 107.0℃ |
Solubilitas | Solutum in Methanol |
Brand | Ruifu Chemical |
Item | Specifications |
Aspectus | Alba ad Off-White pulveris |
Puritas (LC-220nm) | ≥99.0% |
EE (LC) | ≥99.0% |
Imprimis Rotationes | +2.5° ~ +6.5° (C=1, CHCl3). |
una immunditia | ≤0.50% |
Totalis immunditias | <1.00% |
Metalla gravia (ut Pb) | <20ppm |
Test Standard | Enterprise Standard |
Consuetudinem | Chiral Compositions;Pharmaceutical intermedia |
sarcina: Utrem, aluminium foil, pera, cardboard Drum, 25kg/Drum, vel secundum exigentiam emptoris.
Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine, humore et pestis infestatione.
Shanghai Ruifu Chemical Co., Ltd. est primarium fabricae et supplementi (R)-(+)-tert-Butylsulfinamidei (CAS: 196929-78-9) magna qualitate, late in synthesi organica, synthesi intermedia et pharmaceutica Active Pharmaceutical Ingrediens (API) synthesis
Shanghai Ruifu Chemical Co, Ltd. magni ponderis munus agit in chymiae chiralae, societas commissa productioni compositionum chiralium.Nostri fructus a clientibus late laudantur.
(R)-(+)-2-Methyl-2-propanesulfinamide ligandum chirale est, quod in compositionibus pharmaceuticis adhibetur.Ad praeparationem sulfinamides beta-chloro adhibetur in synthesi chiralorum azridinarum.In praeparatione organocatalysi ad enantioselectivam iminum reductionem implicatur.Hoc gerens est ad aminas chiralis componendas.Praeter hoc, in P,N-sulfinyl ligandum imine convertitur per condensationem cum aldehydibus et ketonibus quae iridium catalysatum asymmetricum hydrogenii olefins sustinent.